|
|
||||||||
Radiologic-Pathologic Conference of |
1
Department of Radiology, Keller Army Community Hospital, West Point, NY
10996-1197; Division of Radiologic Sciences, Department of Radiology, Wake
Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC
27157-1088; and Departments of Radiology and Nuclear Medicine, Uniformed
Services University of Health Sciences, 4301 Jones Bridge Rd., Bethesda, MD
20814-4799.
2
Department of Radiology, Madigan Army Medical Center, Bldg. 9040, Fitzsimmons
Dr., Tacoma, WA 98431-0001.
3
Department of Pathology, Madigan Army Medical Center, Tacoma, WA
98431-0001.
Received March 8, 2001;
accepted after revision April 13, 2001.
Address correspondence to L. T. Bui-Mansfield at the West Point
address.
Introduction
|
|
|---|
|
|
|
|
Mesotheliomas are mesenchymal neoplasms originating in the serous lining of the pleura, pericardium, or peritoneum. Multicystic mesothelioma of the peritoneum is an intermediate form of mesothelioma: the severity of the disorder is greater than that of the localized, benign adenomatoid mesothelioma but is less than that of the highly lethal form of diffuse epithelial mesotheliomas [1]. Multicystic mesothelioma occurs predominantly (84% of cases) in young or middle-aged women (mean age, 37 years 10 months) [1, 2]. The tumor chiefly affects the pelvic peritoneum, particularly the uterus, cul-de-sac, bladder, and rectum, growing along the serosa as multiple translucent fluid-filled cysts. Multicystic mesothelioma is made up of mesothelium-lined cysts embedded in fibrovascular stroma. The mesothelial cells are typically flattened or cuboidal. In one third of patients, adenomatoid change or squamous metaplasia of the mesothelium is found [1]. Unlike the malignant form of mesothelioma, multicystic mesothelioma has no association with asbestos exposure [1]. The most common presenting symptoms are abdominal pain (46% of patients) and abdominal mass (29% of patients) [2]. In 18% of patients, the tumor is an incidental finding [2].
On sonography, multicystic mesothelioma appears as a multiseptate cystic mass [3]. Typically, CT reveals a well-defined, noncalcified multilocular cystic mass [2], although a case of calcification in a benign cystic peritoneal mesothelioma has been reported [4]. MR imaging shows well-defined lesions that are hypointense on T1-weighted images and have intermediate signal intensity on T2-weighted images, isointense to urine. This finding correlates with the clear watery fluid seen at gross pathologic examination [2].
Differential diagnoses include lymphangioma, endometriosis, ovarian cystadenoma or cystadenocarcinoma, teratoma, pseudomyxoma peritonei, necrotic leiomyoma or leiomyosarcoma, and epithelial inclusion cysts [1, 2]. Because of the rarity of multicystic mesothelioma, a correct pre-operative diagnosis is almost never rendered [1].
Multicystic mesothelioma is not chemo- or radiosensitive. No correlation exists between the extent of the tumor and the patient's survival. Treatment for localized lesions is total surgical excision, and for more extensive lesions, debulking procedures are performed.
|
|
|---|
This article has been cited by other articles:
![]() |
Y. J. Jeong, S. Kim, S. W. Kwak, N. K. Lee, J. W. Lee, K.-I. Kim, K. U. Choi, and T. Y. Jeon Neoplastic and Nonneoplastic Conditions of Serosal Membrane Origin: CT Findings RadioGraphics, May 1, 2008; 28(3): 801 - 818. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. L. Wong, T. A. Johns, W. G. Herlihy, and H. L. Martin Best Cases from the AFIP: Multicystic Mesothelioma RadioGraphics, January 1, 2004; 24(1): 247 - 250. [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |