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Summary
Sinobronchial syndrome occurs in some cases of paranasal sinus disease. The clinical picture of sinobronchial syndrome
is based on the evacuation of exudate from sinuses to nasopharynx, larynx, and to the lower respiratory tract. Causes
leading to the development of this condition are discussed. The authors, based on their own experience and data from
literature, present the pathogenesis, diagnostic methods, and treatment of sinobronchial syndrome.
INTRODUCTION
In Nelson´s Texbook of Pediatrics we find the following definition of sinobronchial syndrome; „The
term sinobronchitis is occasionally used to designate the relationship between sinus and lower
respiratory tract symptoms; children with this condition may have reactive airways, cystic fibrosis,
immunodeficiency, or dyskinetic cilia as the underlying disease” (2).
The typical clinical view of sinobronchial syndrome has promped many authors to propose the
hypothesis that abnormal defensive mechanism of respiratory tract mucous membrane, and the
incomplete response of the immunological system in children, are underlying pathological mechanisms.
PATHOLOGY
The normal physiological function of the paranasal sinuses depends on 3 main factors: structure and
function of mucous membrane, mucus drainage, and ventilation. Mucociliary transport plays the main
role in the local defensive mechanism of mucous membrane. The predominant immunoglobulin in
mucous is IgA, produced by plasma cells in the submucosa. IgG penetrates from blood vessels by a
passive diffusion mechanism (8).
The immunological system achieves complete efficiency in children at 10-12 years old. That is why
infections of the respiratory tract in children follow a different course than in adults. During the first years
of life a relative immunodeficiency is observed in children compared to adults. Levels of IgG reach adult
values at approximately 3 years of age and IgA levels at 7 to 8 years. Children also have 6 to 7 viral
infections per year. Frequent viral infections may influence the immunological response and lead to an
abnormal immunological reaction. Recurrent viral infection could also impair mucociliary transport (5).
In some children with sinobronchial syndrome, adenoid hypertrophy or septal deviation are
diagnosed (10). These pathological circumstances impair the normal ventilation of the sinuses and lead
to prolongation of the inflammation process.
Studies of immunological processes in recurrent sinusitis in children, carried out in recent years,
confirm the hypothesis about an abnormal immunological response. In a group of children with
sinobronchial syndrome, immunoglobulin A level in serum was found to be reduced to the lower limit of
the norm for the patient´s age (9).
Shapiro and others showed abnormal results of immunological studies, in 34 of 61 children with
chronic sinusitis. Depressed IgG levels and poor response to pneumococcal and Haemophilus
influenzae antigens were found. Twenty-two patients had positive prick tests. These findings, sugges
an allergic component in the pathogenesis of sinusitis in this group of children (11).
Baroody and coworkers compared the structure of mucosa from the sinuses of children suffering
from chronic sinusitis with that obtained from the sphenoid sinuses of healthy adults. There were
significantly more eosinophils in the tissues of children with chronic sinusitis. Allergy status did not affect
the degree of tissue eosinophilia (1).
Driscoll and others, in an investigation carried out in the same way, showed significantly more CD4+
cells in the sinus mucosa of children with chronic sinusitis than in normal sinus mucosa. The number of
CD8+ cells was not significantly different in either group. This contrasts with published results on adults
with chronic sinusitis, in whom CD8+cells predominate in nasal polyps and submucosa. Authors
suggest that this possibly reflects a difference in the immunologic response of children and adults (5).
Predicted these studies explain only a few immunological mechanisms taking place in sinusitis in
children. Further investigations should be carried out to elucitade the immunological processes.
Sinobronchial syndrome usually recurs in a period of exacerbation and remission during a few
succeding years especially in autumn and winter. A cough is the most characteristic symptom. Cough
attacks usually appear one or two hours after the child falls asleep, and also in the morning. During the
day the child is usually free of symptoms, related to the changing position of exudate in relation to the
sinus ostia. No auscultatory pathological signs can be elicited from the bronchial tree (4). The remaining
symptoms of sinobronchial syndrome are typical of other forms of sinusitis in children:
- nasal obstruction,
- headache,
- irritability, tiredness.
DIFFERENTIATION
Sinobronchial syndrome should be differentiated from bronchitis and pneumonitis. In bronchitis and
pneumonitis a cough is steady symptom, and there are typical auscultatory signs. Other causes of
cough are:
- drug-induced cough,
- psychogenic cough,
- other disorders, which stimulate a cough receptor of afferen neurones in the cough reflex arc.
DIAGNOSIS
Diagnosis of sinobronchial syndrome is based on typical clinical symptoms (4). Sometimes we need
to take X-rays of the sinuses and chest to confirm the diagnosis. In patients with frequent recurrences
of sinusitis and bronchitis or pneumonitis it is necessary to exclude diseases which may appear as
sinobronchial syndrome: mucoviscidosis, immotile cilia syndrome and congenital or acquired
immunodeficiency. For this purpose we need to carry out diagnostic examinations such as:
- immunological tests,
TREATMENT
In cases of a patient with sinobronchial syndrome, and with concominant adenoid hypertrophy or
nasal septal deviation, operative treatment should be taken into concideration.
Piśmiennictwo
1. Baroody F.M.et al.: Eosinophilia in Chronic Childhood Sinusitis. Arch. Otolarygol. Head. Neck. Surg. 1995, 121:1396-
1402. 2. Behrman R.E.: Podręcznik Pediatrii. Nelson, pod red. M. Sieniawskiej, Wyd. Naukowe PWN, Warszawa 1996,
str 875. 3. Chazan R.: Zakażenia układu oddechowego. a-medica press, Warszawa 1998, 57-61. 4. Danielewicz J.:
Klinika i patogeneza zespołu zatokowo-oskrzelowego u dzieci. Ped. Pol. 1981, 61:11-12, 1311-15. 5. Driscoll P.V. et al.:
CD4 Lymphocytes Are Increased in the Sinus Mucosa of Children With Chronic Sinusitis. Arch. Otolaryngol. Head. Neck.
Surg. 1996, 122:1071-76. 6.Gul E. et al.: Kilka uwag na temat zapaleń zatok przynosowych u dzieci na podstawie analizy
materiału Oddziału Laryngologii Wojewódzkiego Szpitala we Wrocławiu z lat 1987-1992. Otolaryng. Pol. 1994, 48, supl.,
136139. 7. Kossowska E.: Podsumowanie obrad pierwszego dnia kongresu Otolaryng. Pol. supl., I Europejski Kongres
Otolaryngologii Pediatrycznej 5-7.09.1979 Warszawa, 76. 8. Krzeski A., Janczewski G.: Choroby nosa i zatok
przynosowych. Sanmedia Warszawa 1997, 4849. 9. Łakota A. i wsp.: Poziom magnezu w surowicy i jego wpływ na
leczenie zespołu zatokowooskrzelowego u dzieci. Otolaryng. Pol. 1994, 48, supl. 18, 125-132. 10. Nowak W. et al.:
Zespół zatokowooskrzelowy u dzieci leczonych w Szpitalu Miejskim w Bytomiu w latach 1976-1978. Otolaryng. Pol. supl.
I Europejski Kongres Otolaryngologii Pediatrycznej 57.09.1979 Warszawa, 50-51. 11. Shapiro G.G. et al.: Immunological
Defect in Patients With Refractory Sinusitis Pediatrics 1991, 87, 3:311-16.