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Vitamin A deficiency interfere with rhodopsin production impair rod function Night blindness. Xerophthalmia Fundus disappear within 2--4 months in response to Vitamin A therapy. Cataract Any opacity of the lens that causes diminution or impairment of vision.
Vitamin A deficiency interfere with rhodopsin production impair rod function Night blindness. Xerophthalmia Fundus disappear within 2--4 months in response to Vitamin A therapy. Cataract Any opacity of the lens that causes diminution or impairment of vision.
Vitamin A deficiency interfere with rhodopsin production impair rod function Night blindness. Xerophthalmia Fundus disappear within 2--4 months in response to Vitamin A therapy. Cataract Any opacity of the lens that causes diminution or impairment of vision.
myorganicchemistry.wikispaces.com Retinol elaboration of rhodopsin by the rods the sensory receptors of the retina responsible for vision under low levels of illumination Vitamin A deficiency interfere with rhodopsin production impair rod function Night blindness VITAMIN A DEFICIENCY AND ITS CONSEQUENCES A field guide to detection and control. Alfred Sommer. World Health Organization. Geneva:1995 Conjunctival Xerosis The epithelium of the conjunctiva transformed to the stratified squamous typeLoss of goblet cells, formation of a granular cell layer and keratinization of the surface N columnar cell appears in the temporal quadrant Therapy o resolve within 25 days, most will disappear within 2 weeks Night blindness Responds rapidly, usually within 2448 hours to vitamin A therapy Corneal Xerosis responds within 25 days with the cornea regaining its normal appearance in 12 weeks Xerophthalmia Fundus disappear within 24 months in response to vitamin A therapy VITAMIN A DEFICIENCY AND ITS CONSEQUENCES A field guide to detection and control. Alfred Sommer. World Health Organization. Geneva:1995 http://www.moondrag on.org/health/disorders /xerophthalmia.html 54. REFRACTIVE DISORDER Refractive Disorder Myopia Concave lens. The smallest Dioptri to corret the visual aquity to 6/6 Minus lenses to be used to correct myopia should be no stronger than abso- lutely necessary. Accommodative asthenopia (rapid ocular fatigue) results from the excessive stress caused by chronic con- traction of the atrophic ciliary muscle. 55. Cataract Any opacity of the lens or loss of transparency of the lens that causes diminution or impairment of vision Classification : based on etiological, morphological, stage of maturity Etiological classification : Senile Traumatic (penetrating, concussion, infrared irradiation, electrocution) Metabolic (diabetes, hypoglicemia, galactosemia, galactokinase deficiency, hypocalcemia) Toxic (corticosteroids, chlorpromazine, miotics, gold, amiodarone) Complicated (anterior uveitis, hereditary retinal and vitreoretinal disorder, high myopia, intraocular neoplasia Maternal infections (rubella, toxoplasmosis, CMV) Maternal drug ingestion (thalidomide, corticosteroids) Presenile cataract (myotonic dystrophy, atopic dermatitis) Syndromes with cataract (downs syndrome, werners syndrome, lowes syndrome) Hereditary Secondary cataract http://sdhawan.com/ophthalmology/lens&cataract.pdf E-mail: sdhawan@sdhawan.com Cataract
Sign & symptoms: Near-sightedness (myopia shift) Early in the development of age-related cataract, the power of the lens may be increased Reduce the perception of blue colorsgradual yellowing and opacification of the lens Gradual vision loss Almost always one eye is affected earlier than the other Shadow test +
Morphological classification : Capsular Subcapsular Nuclear Cortical Lamellar Sutural Stage of maturity classification: Immature Mature Intumescent Hypermature Morgagnian Chronological classification: Congenital (since birth) Infantile ( first year of life) Juvenile (1-13years) Presenile (13-35 years) Senile
Katarak Traumatik Paling sering disebabkan oleh cedera benda asing di lensa atau trauma tumpul bola mata Sering mengenai pekerja industri Gejala dan Tanda: Penglihatan kabur mendadak Mata merah Lensa opak Perdarahan intraokular gambaran bintang pada lensa posterior yang dapat dilihat melalui pupil yang dilatasi maksimal Komplikasi : infeksi, uveitis, ablasio retina, glaukoma Tatalaksana : antibiotik sistemik dan topikal, kortikosteroid topikal, katarak dikelurakan pada saat pengeluaran benda asing atau setelah peradangan mereda Inflammatory diseases Ocular toxocariasis Congenital toxoplasmosis Congenital cytomegalovirus retinitis Herpes simplex retinitis Other types of fetal iridochoroiditis Pseudo-uveitis Endophthalmitis Tumors Retinoblastoma Medulloepithelioma Naevoxanthome juvenile Glioneuroma Leukemia Choroidal hemangioma Combined retinal hamartoma Congenital malformations Persistent Hyperplastic Fetal Vasculature (PHFV) Posterior coloboma Retinal fold Myelinated nerve fibres Morning Glory Syndrome X-linked retinoschisis Retinal dysplasia Norries disease Incontinentia pigmenti Phakomatoses Astrocytic hamartoma (Bournevilles tuberous sclerosis) Retinal capillary hemangioma (von Hippel- Lindau) Encephalotrigeminal syndrome (Sturge- Weber) Neurofibromatosis (von Recklinhausen) (NF1 Divers Vitreous hemorrhage Retinal detachment Strabismus (Brckners phenomenon) Stickler syndrome Trauma Contusion of the globe Intraocular foreign body Shaken baby syndrome Vascular diseases Retinopathy of prematurity Coats disease Familial exudative vitreoretinopathy 56. Differential Diagnosis in Pediatric Leukocoria h t t p : / / w w w . n c b i . n l m . n i h . g o v / p m c / a r t i c l e s / P M C 2 7 0 4 5 4 1 /
Retinoblastoma Retinoblastoma (Rb) is a rapidly developing cancer that develops in the cells of retina, the light-detecting tissue of the eye. Caused by a mutation in a gene controlling cell division, causing cells to grow out of control and become cancerous. Signs and Symptoms : The pupil of the eye appears white instead of red when light shines into it (known as "cat's eye reflex" or "white eye"). This may be seen in flash photographs of the patient. The eyes appear to be looking in different directions (crossed eyes). Pain or redness in the eye. An enlarged or dilated pupil Blurred vision or poor vision Different colored irises
Treatment : The priority is to preserve the life of the child, then to preserve vision, and then to minimize complications or side effects of treatment. Treatment options :chemotherapy, cryotherapy, radioactive plaques, laser therapy, external beam radiotherapy and surgical removal of the eyeball (enucleation) Retinoblastoma
Katarak sejenis kerusakan mata yang menyebabkan lensa mata berselaput dan rabun. Lensa mata menjadi keruh dan cahaya tidak dapat menembus Ablasio retina Lepasnya retina sensorik dari RPE akibat adanya robekan, tarikan atau terkumpulnya cairan pada retina. Gejala:vitreous floaters, fotopsia, terhalang pandangan tepi seperti ada tirai Displasia retina an eye disease affecting the retina of animals and, less commonly, humans. It is usually a nonprogressive disease and can be caused by viral infections, drugs, vitamin A deficiency, or genetic defects. Retinal dysplasia is characterized by folds or rosettes (round clumps) of the retinal tissue. Fibroplasia retrolental a disease of the eye affecting prematurely-born babies generally having received intensive neonatal care. It is thought to be caused by disorganized growth of retinal blood vessels which may result in scarring and retinal detachment. Risk factor: prematurity, oxygen toxicity Inflammatory diseases Ocular toxocariasis Congenital toxoplasmosis Congenital cytomegalovirus retinitis Congenital cataract Herpes simplex retinitis Other types of fetal iridochoroiditis Pseudo-uveitis Endophthalmitis Tumors Retinoblastoma Medulloepithelioma Naevoxanthome juvenile Glioneuroma Leukemia Choroidal hemangioma Combined retinal hamartoma Congenital malformations Persistent Hyperplastic Fetal Vasculature (PHFV) Posterior coloboma Retinal fold Myelinated nerve fibres Morning Glory Syndrome X-linked retinoschisis Retinal dysplasia Norries disease Incontinentia pigmenti Phakomatoses Astrocytic hamartoma (Bournevilles tuberous sclerosis) Retinal capillary hemangioma (von Hippel- Lindau) Encephalotrigeminal syndrome (Sturge- Weber) Neurofibromatosis (von Recklinhausen) (NF 1 Divers Vitreous hemorrhage Retinal detachment Strabismus (Brckners phenomenon) Stickler syndrome Trauma Contusion of the globe Intraocular foreign body Shaken baby syndrome Vascular diseases Retinopathy of prematurity Coats disease Familial exudative vitreoretinopathy 57. Differential Diagnosis in Pediatric Leukocoria h t t p : / / w w w . n c b i . n l m . n i h . g o v / p m c / a r t i c l e s / P M C 2 7 0 4 5 4 1 /
Katarak Kongenital Perubahan pada kebeningan struktur lensa mata yang muncul pada saat kelahiran bayi atau segera setelah bayi lahir dengan usia < 1 tahun Unilateral/Bilateral Keruh/buram di lensa terlihat sebagai bintik/bercak putih dan dapat dilihat dengan mata telanjang Faktor resiko :kelainan kromosom, atau gangguan penyakit maternal selama masa kehamilan seperti penyakit metabolis (galaktosemia), infeksi intraurin (rubella pada trimester pertama), pemakaian obat selama kehamilan, toksoplasmosis, DM, hipoparatiroidism Penyulit : makula lutea tidak cukup mendapat rangsangan tidak berkembang sempurna ambliopia sensoris; nistagmus; strabismus Pengobatan : operasi. Ilmu Penyakit Mata, Sidarta Ilyas, 2005 Retinoblastoma Keganasan pada sel retina. Tampak seperti mata kucing/mata memantulkan cahaya putih, pupil tampak membesar Ablasio retina Lepasnya retina sensorik dari RPE akibat adanya robekan, tarikan atau terkumpulnya cairan pada retina. Gejala:vitreous floaters, fotopsia, terhalang pandangan tepi seperti ada tirai Displasia retina an eye disease affecting the retina of animals and, less commonly, humans. It is usually a nonprogressive disease and can be caused by viral infections, drugs, vitamin A deficiency, or genetic defects. Retinal dysplasia is characterized by folds or rosettes (round clumps) of the retinal tissue. Fibroplasia retrolental a disease of the eye affecting prematurely-born babies generally having received intensive neonatal care. It is thought to be caused by disorganized growth of retinal blood vessels which may result in scarring and retinal detachment. Risk factor: prematurity, oxygen toxicity 58. KORNEA uveitis posterior perdarahan vitreous Ablasio retina oklusi arteri atau vena retinal neuritis optik neuropati optik akut karena obat (misalnya etambutol), migrain, tumor otak MATA TENANG VISUS TURUN PERLAHAN MATA TENANG VISUS TURUN MENDADAK MATA MERAH VISUS NORMAL MATA MERAH VISUS TURUN Keratitis Keratokonjungt ivitis Ulkus Kornea Uveitis glaukoma akut Endoftalmitis panoftalmitis Katarak Glaukoma retinopati penyakit sistemik retinitis pigmentosa kelainan refraksi konjungtivitis murni Trakoma mata kering, xeroftalmia Pterigium Pinguekula Episkleritis skleritis ANAMNESIS mengenai media refraksi (kornea, uvea, atau seluruh mata) struktur yang bervaskuler sklera konjungtiva tidak menghalangi media refraksi Corneal Ulcer An inflammatory or more seriously, infective condition of the cornea involving disruption of its epithelial layer with involvement of the corneal stroma (Fluoresens test (+)) Causative Agent Feature Treatment Fungal Fusarium & candida species, conjungtival injection, satellite lesion, stromal infiltration, hypopion, anterior chamber reaction Natamycin, amphotericin B, Azole derivatives, Flucytosine 1% Protozoa infection (Acanthamoeba) associated with contact lens users swimming in pools Viral HSV is the most common cause, Dendritic lesion, decrease visual accuity Acyclovir Staphylococcus (marginal ulcer) Rapid corneal destruction; 24-48 hour, stromal abscess formation, corneal edema, anterior segment inflammation. Centered corneal ulcers. Traumatic events, contact lens, structural malposition Tobramycin/cefazoli n eye drops, quinolones (moxifloxacin) Pseudomonas Streptococcus connective tissue disease RA, Sjgren syndrome, Mooren ulcer, or a systemic vasculitic disorder (SLE) http://emedicine.medscape.com/article/798100 59. RETINOPATI uveitis posterior perdarahan vitreous Ablasio retina oklusi arteri atau vena retinal neuritis optik neuropati optik akut karena obat (misalnya etambutol), migrain, tumor otak MATA TENANG VISUS TURUN PERLAHAN MATA TENANG VISUS TURUN MENDADAK MATA MERAH VISUS NORMAL MATA MERAH VISUS TURUN Keratitis Keratokonjungt ivitis Ulkus Kornea Uveitis glaukoma akut Endoftalmitis panoftalmitis Katarak Glaukoma retinopati penyakit sistemik retinitis pigmentosa kelainan refraksi konjungtivitis murni Trakoma mata kering, xeroftalmia Pterigium Pinguekula Episkleritis skleritis ANAMNESIS mengenai media refraksi (kornea, uvea, atau seluruh mata) struktur yang bervaskuler sklera konjungtiva tidak menghalangi media refraksi RETINOPATI HIPERTENSI Kelainan retina dan pembuluh darah retina akibat tekanan darah tinggi arteri besarnya tidak teratur, eksudat pada retina, edema retina, perdarahan retina Kelainan pembuluh darah dapat berupa : penyempitan umum/setempat, percabangan yang tajam, fenomena crossing, sklerose Pada retina tampak : akibat sklerose (refleks copper wire/silver wire, lumen pembuluh irreguler, fenomena crossing); perdarahan atau eksudat retina (gambaran seperti bintang, cotton wool patches); perdarahan vena (flame shaped) Ilmu Penyakit Mata, Sidarta Ilyas, 2005 CLASSIFICATION SYMPTOMS FEATURE Mild non-proliferative (mild pre-proliferative) None Microaneurysms only, reflects structural changes in the retina Proliferative retinopathy Floaters, sudden visual loss New vessel formation either at the disc (NVD) or elsewhere (NVE), vitreous or preretinal haemorrhage Central and branch retinal artery occlusion Penurunan penglihatan hebat yang tidak nyeri yang terjadi dalam periode beberapa detik. Funduskopi : retina superfisialis mengalami pengeruhan kecuali di foveola cherry red spot Central and branch retinal vein occlusion penurunan penglihatan mendadak yang tidak nyeri perdarahan retina kecil-kecil tersebar dan bercak cotton-wool, dapat juga gambaran perdarahan hebat dengan perdarahan retina superfisialis dan dalam, vena melebar dan berkelok-kelok, edema makula dan retina http://bestpractice.bmj.com/best- practice/monograph/532/basics/classification.html http://medweb.bham.ac.uk/easdec/gradingretinopathy.htm 60-61. KONJUNGTIVITIS Pathology Etiology Feature Treatment Bacterial staphylococci streptococci, gonocci Corynebacteri um strains Acute onset of redness, grittiness, burning sensation, usually bilateral eyelids difficult to open on waking, diffuse conjungtival injection, mucopurulent discharge, Papillae + topical antibiotics Artificial tears Viral Adenovirus herpes simplex virus or varicella- zoster virus
Unilateral watery eye, redness, discomfort, photophobia, eyelid edema & pre-auricular lymphadenopathy, follicular conjungtivitis, pseudomembrane (+/-) Days 3-5 of worst, clear up in 714 days without treatment Artificial tears relieve dryness and inflammation (swelling) Antiviral herpes simplex virus or varicella-zoster virus http://www.cdc.gov/conjunctivitis/about/treatment.html Conjunctivitis is swelling (inflammation) or infection of the membrane lining the eyelids (conjunctiva) Pathology Etiology Feature Treatment Fungal Candida spp. can cause conjunctivitis Blastomyces dermatitidis Sporothrix schenckii Not common, mostly occur in immunocompromised patient, after topical corticosteroid and antibacterial therapy to an inflamed eye Topical antifungal Vernal Allergy Chronic conjungtival bilateral inflammation, associated atopic family history, itching, photophobia, foreign body sensation, blepharospasm, cobblestone pappilae, Horner- trantas dots Removal allergen Topical antihistamine Vasoconstrictors Inclusion Chlamydia trachomatis several weeks/months of red, irritable eye with mucopurulent sticky discharge, acute or subacute onset, ocular irritation, foreign body sensation, watering, unilateral ,swollen lids,chemosis ,Follicles Doxycycline 100 mg PO bid for 21 days OR Erythromycin 250 mg PO qid for 21 days Topical antibiotics
62. Cataract Any opacity of the lens or loss of transparency of the lens that causes diminution or impairment of vision Classification : based on etiological, morphological, stage of maturity Etiological classification : Senile Traumatic (penetrating, concussion, infrared irradiation, electrocution) Metabolic (diabetes, hypoglicemia, galactosemia, galactokinase deficiency, hypocalcemia) Toxic (corticosteroids, chlorpromazine, miotics, gold, amiodarone) Complicated (anterior uveitis, hereditary retinal and vitreoretinal disorder, high myopia, intraocular neoplasia Maternal infections (rubella, toxoplasmosis, CMV) Maternal drug ingestion (thalidomide, corticosteroids) Presenile cataract (myotonic dystrophy, atopic dermatitis) Syndromes with cataract (downs syndrome, werners syndrome, lowes syndrome) Hereditary Secondary cataract http://sdhawan.com/ophthalmology/lens&cataract.pdf E-mail: sdhawan@sdhawan.com
Sign & symptoms: Near-sightedness (myopia shift) Early in the development of age-related cataract, the power of the lens may be increased Reduce the perception of blue colorsgradual yellowing and opacification of the lens Gradual vision loss Almost always one eye is affected earlier than the other Shadow test +
Morphological classification : Capsular Subcapsular Nuclear Cortical Lamellar Sutural Stage of maturity classification: Immature Mature Intumescent Hypermature Morgagnian Chronological classification: Congenital (since birth) Infantile ( first year of life) Juvenile (1-13years) Presenile (13-35 years) Senile
Cataract Treatment : Surgery Cataract surgery is the removal of the natural lens of the eye that has developed an opacification then an artificial intraocular lens implant is inserted Pirenoxine (Catalin) is a medication used in the possible treatment and prevention of cataracts. A report in the journal of Inorganic Chemistry showed that in liquid solutions Pirenoxine could cause decreased cloudiness of a crystallin solution produced to mimic the environment of the eye. Abstract of a research on how pirenoxine (PRX) interacts with selenite or calcium ions that have been proven as factors leading to the formation of lens cataract is available at http://pubs.acs.org/stoken/presspac/presspac/full/10.1021/ic102151p Researchers found that pirenoxine reduced the cloudiness of the lens solution containing calcium by 38 percent and reduced the cloudiness of the selenite solution by 11 per cent. http://en.wikipedia.org/wiki/Pirenoxine Quinolone A family of synthetic broad-spectrum antibacterial drugs Pilokarpine A parasympathomimetic alkaloid, used to treat chronic open- angle glaucoma, acute angle-closure glaucoma Betamethasone Corticosteroid for eye inflammation. Contraindicated in fungal infections and hypersensitivity Hidroksietilselulosa Eye lubricants, for dry and irritated eye 63. TRAUMA Trauma tumpul menyebabkan peningkatan tekanan dalam orbita dan intraokular disertai deformitas bola mata. Tanda: nyeri ringan, kekaburan penglihatan, kemosis hemoragik, laserasi konjungtiva, kamera anterior dangkal dengan atau tanpa dilatasi pupil yang eksentrik, ablasi retina, hifema, atau perdarahan korpus vitreosus Ablasio Retina Ablasio retina adalah suatu keadaan terpisahnya sel kerucut dan batang retina (retina sensorik) dari sel epitel pigmen retina Mengakibatkan gangguan nutrisi retina pembuluh darah yang bila berlangsung lama akan mengakibatkan gangguan fungsi penglihatan Terdapat tiga jenis utama/penyebab ablasio retina yaitu : ablasi retina regmategenosa, ablasi retina traksi (tarikan) dan ablasi retina eksudatif Gejala : vitreous floaters, fotopsia, terhalangnya pandangan tepi seperti ada tirai, metamor-fopsia, dan penurunan visus, Ada semacam tirai tipis berbentuk parabola yang naik perlahan-lahan dari mulai bagian bawah bola mata dan akhirnya menutup pandangan Funduskopi : adanya robekan retina, retina yang terangkat berwarna keabu- abuan, biasanya ada fibrosis vitreous atau fibrosis preretinal bila ada traksi. Bila tidak ditemukan robekan kemungkinan suatu ablasio nonregmatogen Pengobatan: konservatif(untuk nonregmatogen), pneumatic retinopexy, bakel sklera, vitrektomi tertutup
Vaughn DG, Oftalmologi Umum, ed.14 Hifema Blood in the front (anterior) chamber of the eye a reddish tinge, or a small pool of blood at the bottom of the iris or in the cornea Luksasio lensa Dislokasi lensa dapat pada anterior atau posterior. Anterior : penglihatan turun mendadak, sakit yang sangat, muntah, mata merah dengan blefarospasme, injeksi siliar, edema kornea. Posterior : skotoma pada lapang pandang dan gejala afakia Iridosiklitis Radang uvea anterior. Gejala : mata merah, pupil kecil, nyeri, fotofobia, penglihatan turun ringan dan berair Perdarahan vitreum Sering timbul pada penderita DM, hipertensi, dan anemia sabit. Gejala :penglihatan buram tiba-tiba, peningkatan floater/kilatan cahaya 64. Eyelids Disorders Pathology Feature Chalazion (meibomian gland lipogranuloma) Chronic inflamation of Zeis/Meibom gland; when acutely inflammed Painful, warm, swollen, and firm eyelids, granulomatous reaction, lipogranuloma, usually on the upper eyelid and inside the lid, painless nodules, Increased tearing, Sensitivity to light Hordeolum Localized infection or inflammation of the eyelid margin involving hair follicles of the eyelashes (external hordeolum) or meibomian glands (internal hordeolum),Staphylococcal infection; painful, warm, swollen, and tender eyelids, focal collection of PMN cells and necrotic tissue. erythematous, and localized,Purulent material exudates h t t p : / / e n . w i k i p e d i a . o r g / w i k i /
h t t p : / / w w w . n c b i . n l m . n i h . g o v / p u b m e d h e a l t h /
http://www.healblog.net/wp-content/uploads/Hordeolum-and- Chalazion.jpg Chalazion The result of obstruction of the duct of a meibomian gland, which is usually idiopathic, with secondary lipogranulomatous inflammation Epidemiology : higher incidence in seborrheoc dermatitis, rosacea, and DM Clinical features : a pale, round, firm lesion of the lid. Diagnosis : made clinically Treatment : incision of the cyst and removed by curetting. Steroid injection can initiate remission Prognosis : ocaasionally recurrent NEUROLOGI 65. CAUDA EQUINA SYNDROME Cauda equina syndrome (CES) is a rare syndrome that has been described as a complex of symptoms and signslow back pain, unilateral or bilateral sciatica, motor weakness of lower extremities, sensory disturbance in saddle area, and loss of visceral function resulting from compression of the cauda equina. CES occurs in approximately 2% of cases of herniated lumbar discs and is one of the few spinal surgical emergencies. Etiology : tumors, trauma, spinal stenosis, inflammatory conditions Signs : include weakness of the muscles of the lower extremeties innervated by the compressed lumbar roots (often paraplegia), detrusor weaknesses causing urinary retention and post-void residual incontinence, decreased anal tone and consequent fecal incontinence; sexual dysfunction; saddle anesthesia; bilateral (or unilateral) sciatic leg pain and weakness; and absence of ankle reflex. Pain may, however, be wholly absent; the patient may complain only of lack of bladder control and of saddle-anaesthesia, and may walk into the consulting-room. Red Flag Symptoms:(requiring urgent hospitalisation) include sciatic leg pain and/or severe back pain, with altered sensation over saddle area (genitals, uretha, anus, inner thighs), urine retention or incontinence Diagnosis : CT or MRI Treatment : Surgical decompression http://en.wikipedia.org/wiki/Cauda_equina_syndrome 66-67. HEAD INJURY Brain hematoma : a collection of blood within brain tissue. Hematoma inside the cranium is named according to its location: Subdural hematoma: blood collection between brain and dura Epidural hematoma: blood collection between dura and the skull Subarachnoid Hemorrhage: beneath the arachnoid membrane Intracerebral hematoma: blood collection within the brain Subdural Hematoma A collection of blood below the inner layer of the dura but external to the brain and arachnoid membrane. Subdural hematoma is the most common type of traumatic intracranial mass lesion. Usually resulting from tears in bridging veins which cross the subdural space May cause an increase in intracranial pressure (ICP) compression of and damage to delicate brain tissue Characterized on the basis of their size and location and the amount of time elapsed since the inciting event age (ie, whether they are acute, subacute, or chronic) : Acute subdural hematomas: less than 72 hours old and are hyperdense compared with the brain on computed tomography scans. Subacute phase: begins 3-7 days after acute injury; the surgical literature favors 3 days, whereas the radiological literature favors 7. Subacute subdural hematomas are isodense or hypodense compared with the brain. Chronic subdural hematomas are 21 days (3 wk) or older and are hypodense compared with the brain. However, may be mixed in nature, such as when acute bleeding has occurred into a chronic subdural hematoma. Symptoms: gradually increasing headache and confusion. CT Appearance : crescent shape Treatment: depends on the size and rate of growth. Careful monitoring, insertion of small catheher suck the blood, craniotomy removal of hematoma http://emedicine.medscape.com/article/1137207 Epidural Hematomas 70%-80% located in temporoparietal region where skull fractures cross the path of middle meningeal artery or its dural branches May present with lucid period immediately after trauma and a delay before symptoms evident on CT : Lens shaped (biconvex lens) hematomas that do not cross suture lines Crescent shaped density that may run length of skull Subdural hematomas : crescent shaped density that may run length of the skull Subarachnoid Hemorrhage Intracranial Hemorrhage Menurut Penyebab Stroke dibagi : 1. Stroke Hemoragik a. Intra cerebral hemoragik (ICH) OK : Hypertensi, Aneurysma dan arterioveneus Malformasi (AVM) b. Sub Arachnoid Hemoragik (SAH) diagnosis medis : CT brain scan 2. Stroke Non Hemoragik (Iskemik) OK : Arteriosklerosis & sering dikaitkan dengan : DM, Hypercolesterolemia, Asam urat, hyperagregasi trombosit 3. Emboli Sumber dari tronkus di arteria carotis communis di jantung Lepas trombus embolus otak. 68. STROKE Stroke Manifestasi Klinis : Kelumpuhan wajah atau anggota badan (biasanya hemiparese), timbul mendadak Gangguan hemisensorik Perubahan mendadak status mental Afasia; disartria Gangguan penglihatan atau diplopia Ataksia Vertigo, mual, muntah, nyeri kepala Faktor Resiko : Usia Riw. TIA atau stroke Peny. Jantung koroner Hipertensi DM Merokok Dislipidemia
Intracerebral Hemorrhage Bleeding into brain tissue Usually caused by chronic hypertension Non-hypertension cause more likely if: No past history of hypertension Lobar (i.e., peripheral, not subcortical) May require emergency surgery Accounts for 10% of strokes Hemorrhage: Symptoms only suggestive of hemorrhage. CT or LP needed for definitive diagnosis Headache Neck stiffness Neck pain Light intolerance Nausea, vomiting Decreased consciousness
Pada kasus ini tidak didapatkan tanda- tanda kemungkinan stroke hemoragik jadi kemungkinan yang terjadi adalah stroke iskemik 69. HEADACHE
MIGRAINE 70. MENINGITIS Meningitis: radang pada selaput otak yang melapisi otak dan sumsum tulang belakang Manifestasi klinis : nyeri kepala, dapat menjalar ke tengkuk dan punggung, kaku kuduk, kernig (+), brudzinsky (+) Klasifikasi (berdasarkan perubahan pada cairan otak) : Meningitis serosa : cairan otak jernih, paling sering disebabkan oleh Mycobacterium tuberculosa, penyebab lain: virus, toxoplasma gondhii, ricketsia Meningitis purulenta : cairan mengandung pus, penyebabnya antara lain diplococcus pneumoniae, neisseria meningitidis, streptococcus haemolyticus, staphylococcus aureus, haemophilus influenza, pseudomonas aeruginosa Kapita Selekta Meningitis TB Meningitis TB-Diagnosis Tuberculous meningitis (TBM) is an inflammation of the meninges covering the brain and spinal cord caused by infection with mycobacteria, most usually Mycobacterium tuberculosis. The condition usually presents with headache, fever, and convulsions and is diagnosed clinically, with confirmation by microscopy and culture of cerebrospinal fluid. CSF Examination Usually lymphocytic pleocytosis Paradoxic change from lymphocytic to neutrophilic predominance over 48 hr pathognomonic for TB meningitis Elevated protein with severely depressed glucose Repeated specimens for AFB culture necessary Other Studies Brain imaging demonstrates hydrocephalus, basilar exudates and inflammation, tuberculoma, cerebral edema, cerebral infarction CXR Abnormal, sometimes miliary pattern Treatment
CSF Findings in Meningitis 71. EPILEPSI A seizure is defined by release of excessive and uncontrolled electrical activity in the brain. Seizures themselves are not a disease, they are an event. Epilepsy (seizure disorder) is a neurological condition, that in different times produce brief disturbances in the electrical functions of the brain. Seizures are a symptom of epilepsy. Epilepsy - Classification Focal seizures account for 80% of adult epilepsies - Simple partial seizures - Complex partial seizures - Partial seizures secondarilly generalised
Generalised seizures
Unclassified seizures Partial Seizure Simple Seizure activity in the brain causing: Rhythmic movements - isolated twitching of arms, face, legs Sensory symptoms - tingling, weakness, sounds, smells, tastes, feeling of upset stomach, visual distortions Psychic symptoms - dj vu, hallucinations, feelings of fear or anxiety Usually last less than one minute May precede a generalized seizure Complex Characterized by altered awareness Confusion, inability to respond Automatic, purposeless behaviors such as picking at clothes, chewing or mumbling. Emotional outbursts May be confused with: Drunkenness or drug use Willful belligerence, aggressiveness
GENERALIZED SEIZURES INVOLVE WIDE AREAS OF THE BRAIN AND LOSS OF CONSCIOUSNESS PETIT MAL : CONSCIOUSNESS IS TRANSIENTLY LOST AND THE EEG DISPLAYS SPIKE AND WAVE ACTIVITY GRAND MAL : CONSCIOUSNESS LOST FOR A LONGER PERIOD AND THE INDIVIDUAL WILL FALL IF STANDING WHEN SEIZURE STARTS. TONIC PHASE: GENERALIZED INCREASED MUSCLE TONE. CLONIC PHASE: SERIES OF JERKY MOVEMENTS. BOWEL AND BLADDER MAY EVACUATE.
Epilepsi-Klasifikasi (etiologi) Idiopatik epilepsi : biasanya berupa epilepsi dengan serangan kejang umum, penyebabnya tidak diketahui. Pasien dengan idiopatik epilepsi mempunyai inteligensi normal dan hasil pemeriksaan juga normal dan umumnya predisposisi genetik. Kriptogenik epilepsi : Dianggap simptomatik tapi penyebabnya belum diketahui. Kebanyakan lokasi yang berhubungan dengan epilepsi tanpa disertai lesi yang mendasari atau lesi di otak tidak diketahui. Termasuk disini adalah sindroma West, Sindroma Lennox Gastaut dan epilepsi mioklonik. Gambaran klinis berupa ensefalopati difus. Simptomatik epilepsi : Pada simptomatik terdapat lesi struktural di otak yang mendasari, contohnya oleh karena sekunder dari trauma kepala, infeksi susunan saraf pusat, kelainan kongenital, proses desak ruang di otak, gangguan pembuluh darah diotak, toksik (alkohol, obat), gangguan metabolik dan kelainan neurodegeneratif.
Diagnosis Epilepsi Lengkap-Perdossi 72. PARESE N. VII Menurut Penyebab Stroke dibagi : 1. Stroke Hemoragik a. Intra cerebral hemoragik (ICH) OK : Hypertensi, Aneurysma dan arterioveneus Malformasi (AVM) b. Sub Arachnoid Hemoragik (SAH) diagnosis medis : CT brain scan 2. Stroke Non Hemoragik (Iskemik) OK : Arteriosklerosis & sering dikaitkan dengan : DM, Hypercolesterolemia, Asam urat, hyperagregasi trombosit 3. Emboli Sumber dari tronkus di arteria carotis communis di jantung Lepas trombus embolus otak. 73. STROKE Tatalaksana Khusus Stroke Hemoragik : Perawatan di ICU jika didapatkan volume hematoma lebih dari 30 cc, perdarahan intraventrikuler dengan hidrosefalus dan klinis cenderung memburuk, Tekanan darah diturunkan sampai tekanan darah premorbid atau sebanyak 15-20% bila tekanan sistolik >180, diastolik >120, MAP >130, dan volume hematoma bertambah. Bila terdapat gagal jantung maka tekanan darah segera diturunkan dengan labetolol intravena dengan dosis 10 mg (pemberian dalam 2 menit) sampai 20 mg (pemberian dalam 10 menit) maksimum 300 mg; enelapril intravena 0,625-1.25 mg per 6 jam; Captopril 3 kali 6,25-25 mg peroral, Jika didapatkan tanda-tanda tekanan intra kranial meningkat, maka posisi kepala dinaikkan 30 derajat, dengan posisi kepala dan dada pada satu bidang, bisa dilakukan pemberian manitol (lihat stroke iskemik), dan hiperventilasi (PCO2 20-35 mmHg),
Kapita Selekta Kedokteran 74. CRANIAL NERVES 75. VERTIGO the illusion that the environment is spinning a subtype of dizziness, where there is a feeling of motion when one is stationery Classification : Peripheral Central Common Causes: 1.Peripheral Physiological (motion sickness) Benign paroxysmal positional vertigo (BPPV) most common Vestibular neuronitis Labyrinthitis Menire disease Perilymph fistula 2.Central Brainstem TIA/infarct Posterior fossa tumors Multiple sclerosis Syringobulbia Arnold - Chiari deformity Temporal lobe epilepsy Basilar migraine 3.OtherCardiac, GI, psycogen, toxins, medications, anemia, hypotension Vertigo Peripheral vertigo : caused by problems within the inner ear/vestibular system; also called otologic or vestibular vertigo. The most common cause : BPPV (32%)
Central vertigo : arises from injury to the balance centers of the CNS; less prominent movement illusion and nausea. Has accompanying neurologic deficits (e.g. slurred speech and double vision), and pathologic nystagmus (pure vertical/ torsional) BPPV A clinical syndrome characterized by brief recurrent episodes of vertigo triggered by changes in head position with respect to gravity. Meniere disease An inner ear disorder that causes one to experience periods of vertigo, dizziness, nausea, ear pressure, sensitivity to light and tinnitus Migraine with aura Suatu kondisi kronis dengan karakteristik sakit kepala episodik unilateral yang didahului dengan gejala aura (gangguan visual, sensasi abnormal pada kulit, mual, muntah, dll) 76. PARKINSON DISEASE Parkinson Disease : a degenerative disorder of the central nervous system. The motor symptoms of Parkinson's disease result from the death of dopamine-generating cells in the substantia nigra, a region of the midbrain; the cause of this cell death is unknown. 3 main symptoms: Tremors Rigidity Slowed motion (Bradykinesia) Other symptoms include: Dementia, sleep disturbances, depression, etc.
Parkinson Disease No definitive tests for PD. PET scans can aid to determine levels of dopamine. Medical history and neurological tests are conducted to diagnose. Usually, if two of the cardinal symptoms are present Treatment can be divided into two stages. Early and Later stages Early stage Onset of symptoms, treated with physical therapy and medications (Levodopa, dopamine agonists, etc) Later stage Usually after having received 5+ years of levodopa treatment. Wearing-off and On/Off effect develops, other medication in conjunction levodopa is commenced. MAO-B and COMT inhibitors. 73 Treatment Physical Therapy Regular exercise Recommended throughout the life of disorder. Helps maintain and improve mobility and strength. Physical exercise aids in rigidity relief, muscle strength and flexibility, balance, etc. Caution is advised to avoid sudden movements or strenuous activities fall could result in serious injury.