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Peritoneal Calcification: Causes and


Distinguishing Features on CT
Atul Agarwal1 OBJECTIVE. We undertook this study to determine the causes of peritoneal calcification
Benjamin M. Yeh seen on CT and to investigate which CT features distinguish benign from malignant perito-
Richard S. Breiman neal calcification.
Aliya Qayyum MATERIALS AND METHODS. Seventeen patients with peritoneal calcification were
identified through retrospective review of reports from 74,765 abdominopelvic CT examina-
Fergus V. Coakley
tions performed during a 7-year period. We determined the cause of peritoneal calcification
by examining medical and histopathologic records. Calcification morphology was classified
as nodular or sheetlike on the basis of the consensus interpretation by two independent radiol-
ogists. The radiologists also recorded the presence or absence of associated soft-tissue com-
ponents or lymph node calcification. The association between the CT findings and the cause
of calcification was assessed using chi-square analysis.
RESULTS. Peritoneal calcification was due to peritoneal dialysis (n = 4), prior peritonitis
(n = 3), cryptogenic origin (n = 1), or peritoneal spread of ovarian carcinoma (n = 9). Sheet-
like calcification was more common in patients with benign calcification (seven of eight pa-
tients) than in those with malignant calcification (two of nine patients, p < 0.05). Nodal
calcification was seen only in patients with malignant calcification (five of nine patients vs
none of eight, p < 0.05).
CONCLUSION. Common causes of peritoneal calcification are dialysis, prior peritoni-
tis, or ovarian cancer; sheetlike calcification indicates a benign cause, whereas associated
lymph node calcification strongly suggests malignancy.

T he detection of peritoneal calcifi-


cation on CT is rare but potentially
of major clinical importance be-
cause such findings have been associated with
investigate which CT features distinguish be-
nign from malignant peritoneal calcification.

primary and secondary peritoneal malignan- Materials and Methods


cies [1, 2], as well as with benign causes such Subjects
as sclerosing peritonitis due to peritoneal dial- Ours was a retrospective single-institution study
ysis [3, 4], peritoneal tuberculosis [5], prior approved by our institutional review board. In-
meconium peritonitis [6], hyperparathyroid- formed consent was not required. We performed a
ism [7], Pneumocystis carinii infection [8], computerized search of our radiology information
and postsurgical heterotopic ossification [9]. system (IDXrad software, version 9.7.1, IDX Sys-
Prior case reports and series describing perito- tems, Burlington, VT) for the period January 1995
neal calcification have focused on specific sin- to September 2002 to identify patients whose ab-
Received May 30, 2003; accepted after revision
August 21, 2003. gle causes, but the relative frequency of these dominopelvic CT reports (74,765 examinations)
contained the character strings “periton” and “calc.”
1
All authors: Department of Radiology, University of entities and the potential distinguishing CT
An attending radiologist with subspecialist experi-
California San Francisco, 505 Parnassus Ave., M372, features of benign and malignant calcification
San Francisco, CA 94143-0628. Address correspondence ence in abdominal imaging reviewed the CT studies
have not been studied in a comparative fash- (n = 59) identified in this search to select those
to B. M. Yeh.
ion, although such information would be of cases with definite peritoneal calcification. Perito-
AJR 2004;182:441–445
value to the interpreting radiologist. Therefore, neal calcification was defined as the presence of one
0361–803X/04/1822–441 we undertook this study to determine the cause or more lesions showing CT attenuation similar to
© American Roentgen Ray Society of peritoneal calcification seen on CT and to that of bone in an unequivocally intraperitoneal lo-

AJR:182, February 2004 441


Agarwal et al.

cation such as the perihepatic space, perisplenic Image Interpretation and Analysis patient was performed to treat a low-grade 1.5-
space, paracolic gutters, Morison’s pouch, omental Two attending radiologists reviewed all CT cm renal cell carcinoma with no evidence of
surface, and pouch of Douglas. Many cases were scans and made interpretations by consensus, un- metastatic spread. For each of these patients,
associated with ascites, which frequently facilitated aware of clinical or histopathologic findings. The the extent of peritoneal calcification was
localizing a calcified lesion as intraperitoneal. interpreters classified calcification morphology as greater than that of the expected surgical field.
On the basis of this review, 17 patients were con- nodular (circumscribed and focal) or sheetlike (flat,
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sidered to have had peritoneal calcification. The fi-


The three patients with peritoneal calcifica-
curvilinear, and extending along a peritoneal
nal study group consisted of 14 women and three tion resulting from prior peritonitis also had
plane). Both patterns were recorded if simulta-
men whose mean age was 54 years (range, 30–83 neously present in the same patient. The interpret-
complex histories. One had a history of multi-
years). To determine the cause of peritoneal calcifi- ers also recorded the presence or absence of ple abdominal abscesses and enterocutaneous
cation in these patients, two of the authors reviewed associated soft-tissue components and lymph node fistulas after undergoing a colectomy and co-
all available medical records and recorded pertinent calcification (Figs. 1–3). Soft-tissue components lostomy for perforating diverticulitis. One had
histopathologic and clinical findings, including were considered to be present if structures with CT a history of pancreatitis, endometriosis, chole-
prior surgery, peritoneal dialysis, peritonitis, or con- densities of between 20 and 80 H were observed as cystectomy, appendectomy, hysterectomy, bi-
firmed malignancy (before or after the CT examina- being contiguous to the calcification without an in- lateral salpingo-oophorectomy, and multiple
tion). Calcification was considered benign if tervening fat plane and separate from adjacent or- laparotomies for an adhesive small-bowel ob-
patients had a history of peritoneal calcification gans. The association between CT findings and
known to have a benign cause and no histopatho-
struction. The third patient had a history of
cause was assessed using chi-square analysis. A p
logic evidence of peritoneal malignancy. Calcifica- cholecystectomy and duodenal resection for a
value less than 0.05 was considered to be significant.
tion was considered malignant if patients had duodenal adenoma. The patient with benign
proven peritoneal carcinomatosis. cryptogenic peritoneal calcification exhibited
perihepatic calcifications on CT and had a his-
Results
CT Technique tory of renal transplantation for focal and seg-
Causes of Peritoneal Calcification mental glomerulosclerosis but had no history
CT scans were obtained using helical CT scanners
(LightSpeed [n = 8 patients] or HiSpeed [n = 9 pa- Eight patients had benign peritoneal calcifi- of peritonitis, peritoneal dialysis, other abdom-
tients] General Electric Medical Systems, Milwaukee, cation related to peritoneal dialysis (n = 4), inopelvic surgery, or malignancy.
WI). Sixteen patients received 150 mL IV iohexol peritonitis (n = 3), or cryptogenic origin (n = Nine patients had malignant peritoneal calci-
(Omnipaque 350, Nycomed Amersham, Princeton, 1). Of the four patients who had peritoneal cal- fication. In eight of these patients, calcification
NJ). Sixteen patients received 800 mL oral diatrizoate cification stemming from peritoneal dialysis, was due to peritoneal spread of ovarian cancer
meglumine (Hypaque, Nycomed Amersham). Two
three had documented histories of both dialy- and in one, it was due to primary papillary se-
patients received 250 mL rectal diatrizoate meglu-
sis-related peritonitis and abdominal surger- rous peritoneal carcinoma. Five of the patients
mine (Hypaque). Slice collimation was 5 (n = 8), 7
(n = 6), 8 (n = 1), or 10 (n = 2) mm. All images were ies—cholecystectomy and ventral hernia with ovarian cancer had serous cystadenocarci-
contiguous. Indications for CT scanning were evalua- repair with omentectomy in one patient, chole- noma; for three patients, the histopathologic
tion of abdominal symptoms (n = 7) or of known or cystectomy in another, and partial nephrec- type was unspecified. Lymph node calcification
suspected tumor (n = 10). Abdominal symptoms con- tomy and two failed renal transplantations in was seen in five (56%) of these nine patients.
sisted of pain, nausea, or vomiting. the third. The partial nephrectomy in this latter Eight of the patients had undergone total ab-

A B

Fig. 1.—84-year-old woman with serous ovarian adenocarcinoma.


A, IV and oral contrast–enhanced abdominal CT scan shows large nodular calcifications (arrowheads) in left side of abdomen.
B, Pelvic CT scan shows calcified left inguinal lymph node (arrow). Pelvic cavity is largely replaced by large solid and cystic calcified mass.

442 AJR:182, February 2004


CT of Peritoneal Calcification
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A B
Fig. 2.—30-year-old woman who was undergoing continuous ambulatory peritoneal dialysis.
A, IV and oral contrast–enhanced abdominal CT shows sheetlike calcification around spleen (arrow) and liver (arrowheads) extending into fissure for ligamentum teres.
Splenic arterial calcification is present.
B, Pelvic CT scan shows peritoneal dialysis catheter (white arrow) as well as sheetlike calcification surrounding bowel and mesentery (arrowheads), associated with dif-
fuse bowel wall thickening and soft-tissue components (black arrow).

dominal hysterectomy, bilateral salpingo- Distinction Between Benign and Malignant Peritoneal lignant calcification (two of nine). Nodal calci-
oophorectomy, omentectomy, and lymph node Calcification fication was seen only in patients with
dissection before undergoing CT, and three had The clinical and CT characteristics of pa- malignant calcification (five of nine vs none of
received chemotherapy. One patient with malig- tients with benign and malignant peritoneal eight, p < 0.05). Combining findings of sheet-
nant peritoneal calcification had previously re- calcification are shown in Table 1. Sheetlike like calcifications and absence of nodes or
ceived radiation therapy, and none of the calcification was significantly more common other permutations of findings was not helpful
patients with benign peritoneal calcification had (p < 0.05) in patients with benign calcification in distinguishing patients with benign calcifi-
previously received radiation therapy. (seven of eight patients) than in those with ma- cation from those with malignant calcification.

A B

Fig. 3.—46-year-old woman with ovarian papillary serous adenocarcinoma.


A, IV and oral contrast–enhanced CT scan shows several nodular calcifications (arrows) in lesser sac and fissure for ligamentum teres.
B, Pelvic CT scan shows calcified solid and cystic mass in cul-de-sac caused by disease recurrence.

AJR:182, February 2004 443


Agarwal et al.

Clinical and CT Characteristics in 17 Patients with Benign Versus Malignant cology service are for gynecologic oncology
TABLE 1 patients, and the lack of malignancies other than
Peritoneal Calcification
ovarian or primary papillary serous peritoneal
Cause of Peritoneal Calcification
carcinoma causing peritoneal calcification in
Parameter Benign Malignant p our series is not likely to be due to merely a dis-
(n = 8) (n = 9)
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proportionate number of patients with ovarian


Patients carcinoma at our hospital. The proportion of pa-
Mean age (yr) 50 58 NS tients in our study with ovarian cancer, perito-
neal calcification, and concurrent calcified
Sex ratio (men:women) 3:5 0:9 NS
lymph nodes (5/9 or 56%) was higher than that
Clinical history
reported by Mitchell et al. [1], who described
Peritoneal dialysis 4 0 NS
calcified lymph nodes in only one of six such
Peritoneal infection, inflammation, or surgery 7 8 NS patients (17%). The apparent increased preva-
Ovarian or primary peritoneal cancer 0 9 < 0.05 lence of calcified lymph nodes in our series may
CT features reflect improvement in CT technology since
Nodular calcification 8 9 NS 1986. Much like serous ovarian adenocarci-
Sheetlike calcification 7 2 < 0.05 noma, primary papillary serous peritoneal carci-
Soft-tissue component 4 7 NS noma is known to cause calcified peritoneal
Nodal calcifications 0 5 < 0.05 carcinomatosis and lymph node calcification
Ascites 4 2 NS [2].
Meconium peritonitis is the most common
Note.—NS = not significant.
cause of peritoneal calcification and can cause
microscopic and macroscopic calcified deposits
Discussion or postsurgical changes. However, it is surpris- with varied appearances [6, 22–24], but perito-
Peritoneal calcification is occasionally seen ing that we found lymph node calcification as- neal calcification associated with numerous
on CT of the abdomen and pelvis and has many sociated only with malignancy and not with other entities has been described in several re-
different causes [1–9]. To our knowledge, dis- infectious or inflammatory causes such as tu- ports. In one series, two of the three patients
tinguishing features of these calcifications in re- berculosis or fungal infection. This finding may with AIDS and extrapulmonary Pneumocystis
gard to causation have not been previously reflect, to some extent, the patient population at carinii infections had calcifications of multiple
evaluated. In this study, we sought to find fea- our institution or may reflect the rarity of perito- lymph nodes; one of these two patients had con-
tures of peritoneal calcification that may sug- neal calcification in infectious calcified nodal current small nodular calcifications of the pleu-
gest either a benign or malignant cause. In our disease. This notion is supported by several ral and peritoneal surfaces [8]. Three case
series, we found that peritoneal calcification as- large studies of abdominal tuberculosis that have reports of diffuse nodular peritoneal calcified
sociated with calcified lymph nodes was signifi- reported CT findings of calcified nodal disease deposits of varying sizes, all attributed to tuber-
cantly more likely to be seen in malignancy but have not reported any case of peritoneal calci- culosis, were found at laparoscopy (n = 2) and
than in benign disease and that a sheetlike ap- fication [11–16]. We are aware of only three case autopsy (n = 1) [5, 17, 18]. In one case report of
pearance of peritoneal calcification was associ- reports of peritoneal calcification associated with peritoneal mesothelioma, diffuse peritoneal cal-
ated significantly more frequently with benign tuberculosis, and in each of these case reports, the cification was reported [25], whereas in another
disease. However, although sheetlike peritoneal association with tuberculosis was made by exclu- case report of benign cystic peritoneal mesothe-
calcification suggests a benign rather than ma- sion: no acid-fast bacteria or granulomas were lioma, a large intraperitoneal cystic mass with
lignant cause, this rule should also be applied identified at histology in the calcified peritoneal nodular calcifications was described [26]. A
with caution because a substantial portion (2/9 deposits of these patients [5, 17, 18]. case report of diffuse peritoneal amyloidosis de-
or 22%) of the patients with malignant calcifica- We did not identify peritoneal calcification scribed omental and peritoneal thickening with
tion also had sheetlike calcification. Other char- associated with any malignancy apart from ova- nodular calcifications as well as retroperitoneal
acteristics of peritoneal calcification, including rian cancer or primary papillary serous perito- lymph node calcification [27].
location, size, extent, and association with soft- neal carcinoma. Although some malignancies, Our study has a number of limitations.
tissue masses, were not helpful in distinguishing such as squamous cell lung cancer, renal cell Characteristics of our study population may
benign from malignant causation. carcinoma, and melanoma, are known to induce not allow our findings to be extrapolated to the
Peritoneal calcification is caused by two pri- paraneoplastic hyperparathyroidism and hyper- general population. Although none of our pa-
mary mechanisms. Metastatic calcification may calcemia [19] and could conceivably mimic a tients with benign peritoneal calcification had
be a result of a systemic mineral imbalance in benign pattern of peritoneal calcification, we lymph node calcification, none had a history
entities such as uremia or hyperparathyroidism, did not observe such an occurrence. Other ma- of tuberculosis or P. carinii infection, entities
whereas dystrophic calcification may result lignancies may also cause calcified peritoneal that have been associated with calcification of
from tissue injury, aging, or disease, including carcinomatosis, colon cancer [20], and gastric both lymph nodes and the peritoneum [5, 8].
malignancy [10]. It is not surprising that malig- cancer [21], but we did not find such calcified Other noninfectious benign entities, such as
nant disease is more likely to cause lymph node peritoneal masses in this series. Our institution amyloid and systemic sclerosis, have also been
involvement, and hence lymph node calcifica- serves a large oncology population, but less than associated with calcified lymph nodes [28, 29]
tion, than is renal failure, hyperparathyroidism, 20% of the CT examinations ordered by the on- and potentially the concurrent presence of

444 AJR:182, February 2004


CT of Peritoneal Calcification

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