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Desmoplastic small round cell tumor

Desmoplastic small round cell tumor is classified as a soft tissue sarcoma. It is an aggressive and rare tumor that primarily occurs as multiple masses in the abdomen. Other areas affected include the lymph nodes, the lining of the abdomen, diaphragm , and the pelvis. The most common site of metatastic spred is to the liver, lungs, and bones. more...

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The tumor predominately strikes teenagers and young adults. It usually affects males, more than females.

There is no known risk factors that have been identified specific to the disease. Research has indicated that there is a relationship between desmoplastic small round cell tumor and the Ewings Family of Tumors.

DSRCT is associated with a unique chromosomal translocation (t11;22)(p13:q12) resulting in a chimeric EWS/WTI transcript that is diagnostic of this tumor. This transcript codes for a protein that acts as a transcriptional activator that fails to suppress tumor growth.

Symtoms of disease include abdominal pain, abdominal mass, gastrointestinal obstruction, ascites, possible anemia, and cachexia.

Pathology reveals well circumscribed solid tumor nodules within a dense desmoplastic stroma. Often areas of central necrosis are present. Tumor cells have hyperchromatic nuclei with increased nuclear/cytoplasmic ratio.

On immunohistochemistry, these cells have trilinear coexpression including the epithelial marker cytokeratin, the mesenchymal markers desmin and vimentin, and the neuronal marker neuron-specific enolase. Thus, although initially thought to be of mesothelial origin due to sites of presentation, it is now hypothesized to arise from a progenitor cell with multiphenotypic differentiation.

At this time, the prognosis for desmoplastic small round cell tumor is poor, less than 20%. Usually, by the time the disease is diagnosed the tumor has already grown large within the abdomen and metastasized or seeded to other parts of the body.

Although the tumors are described as chemo-resistant, there is treatment for the disease. Recent journals have reported that some patients respond to high dose chemotherapy, debulking operation , and radiation therapy. Other treatment options considered include: Autologous Stem cell Transplant, Intensity-Modulated Radiation Therapy, Stereotactic Body radiation therapy, and Intraperitoneal hyperthermic chemoperfusion.

This disease is also known as: Desmoplastic small round blue cell tumor; Intraabdominal desmoplastic small round blue cell tumor; Desmoplastic small cell tumor; Desmoplastic sarcoma; DSRCT.


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Pathologic Quiz Case: A 79-Year-Old Woman With a Black, Ulcerated Cecal Tumor and 3 Negative Guaiac Test Results
From Archives of Pathology & Laboratory Medicine, 1/1/05 by Wang, Lina

A 79-year-old woman complained of increasing fatigue with a few episodes of dizziness. Past medical history included hypertension, total hysterectomy at the age of 37 years for a fibroid uterus, and appendectomy at the age of 16 years. The patient reported she was taking the combination product hydrochlorothiazide and triamterene (Dyazide), propranolol, vitamins, and iron. She had smoked since the age of 20 years, 2 packs per day for 50 years. She said she drank one cocktail of vodka and a glass of wine daily. Physical examination revealed pallor and a right abdominal mass. On colonoscopy, she had a large, black, ulcerated cecal mass. Computed tomography scan revealed no métastases. Three guaiac test results were negative for heme. Her white blood cell count was 12600 cells/mm^sup 3^ with a differential of 84% neutrophils, 9% lymphocytes, and 7% monocytes. Other laboratory values included the following: hemoglobin, 8.8 g/dL; hematocrit, 27%; mean corpuscular volume, 67.5 (L^sup 3^; red blood cell distribution width, 18.1%; platelet count, 0.533 × 10^sup 3^/ µL protein, 5.8 g/dL; and albumin, 2.9 g/dL. The carcinoembryonic antigen level was 13.9 ng/mL before surgery. Right hemicolectomy was performed. A 9.0 × 8.5 × 8.0-cm, tar-black tumor mass with extensive ulcération was present in the cecum (Figure 1). The mucosal surface surrounding the base of the large mass was thickened and ragged. Histopathologic sections of the ulcer showed syncytial solid sheets of tumor with rare lumen formation, punctuated by extensive areas of necrosis (Figure 2, original magnification ×40) and covered by numerous grampositive and gram-negative bacilli. sections revealed medium-to-large neoplastic cells with round-to-oval nuclei having clumped to vesicular chromatin and 1 to 3 variably prominent nucleoli with moderate amounts of eosinophilic cytoplasm (Figure 3, original magnification ×400). Ten mitotic figures per 10 high-power fields were identified. The malignant cells were strongly positive for cytokeratin (CK) 20 (Figure 4) and negative for CK7, SlOO, Melan-A, and vimentin. A minimal desmoplastic stromal reaction heavily infiltrated by lymphocytes and plasma cells surrounded the tumor. One of 25 lymph nodes contained a 0.2-cm focus of carcinoma; this node was located immediately adjacent to the main tumor mass.

What is your diagnosis?

Pathologic Diagnosis: Medullary Adenocarcinoma of the Colon, Poorly Differentiated

Medullary adenocarcinoma (MAC) of the colon is a subtype of poorly differentiated colon adenocarcinoma. Often patients with this type of rumor are elderly women with mainly right-sided tumors, either in the cecum or proximal colon, composed of predominantly solid sheets of malignant cells, minimal or no glandular differentiation, little cellular pleomorphism, and peritumoral lymphocytic infiltrate.1-5 Early in 1977, Gibbs4 described an undifferentiated carcinoma that tended to grow large before symptoms were produced but that patients with this carcinoma nevertheless had a good prognosis when it was locally resectable. Appleman1 described these tumors as lymphoepithelioma-like carcinomas, invariably poorly differentiated, and often huge, with no or very few nodal metastases, considering the size of the tumor. The significantly different clinicopathologic features of MAC of the colon are proximal location, large size, invasive into adjacent organs, expanding pattern of growth, low incidence of distant métastases, conspicuous peritumoral lymphocytic involvement, and Crohn-like lymphoid reaction.5 Microscopically, the tumor consists of nests, trabecula, and sheets of small- to medium-sized cells with scant-to-abundant eosinophilic cytoplasm. Some cells contain mucin vacuoles. The nuclei have an open chromatin pattern and exhibit prominent nucleoli and frequent mitotic figures. Lymphatic permeation in the stroma is present in most cases. Dolcetti et al6 found that the lymphocytes in the epithelial compartment of the tumors were predominantly CD8^sup +^ T-cell receptor β cells and express perforin, a molecule that participates in one mechanism of cell killing. Immunohistochemical findings are positive cytokeratin, carcinoembryonic antigen, and epithelial membrane antigen but negative p53.57 Most MACs are DNA diploid by flow cytometric analysis. In addition, young patients with MACs often have a family history highly suggestive of a hereditary background. Most MACs are strongly associated with widespread microsatellite instability (MSI-H).5,7 Medullary adenocarcinomas show high specificity for MSI-H status (99%; P

In this case, the large, black, ulcerated cecal tumor (9.0 × 8.5 × 8.0 cm) showed syncytial solid sheets of malignant cells with minimal gland formation and extensive necrosis. The neoplastic cells were medium to large with round or oval nuclei having clumped to vesicular chromatin and 1 to 3 variably prominent nucleoli with a moderate amount of eosinophilic cytoplasm. Mitotic figures were increased to approximately 10 per 10 high-power fields. The malignant cells are strongly positive for CK20 and carcinoembryonic antigen but negative for CK7, SlOO, Melan-A, p53, CD117 (c-Kit), epidermal growth factor receptor, and vimentin. The tumor cells did not express p53. Numerous lymphocytes and plasma cells permeated the minimal desmoplastic stroma and expressed mostly CD3 with some of them having CDS positivity (Table).

It is important to recognize the difference between MAC and poorly differentiated colonie adenocarcinoma. These 2 tumors are markedly different in their histologic features, phenotype, genotype, and prognosis. Histologically, the medullary-type tumors snowed uniform cells with expansile growth pattern and a dense peritumoral lymphoid infiltrate. These tumors had less frequent lymph node and hematogenous metastases than poorly differentiated colonie adenocarcinoma.8 In addition, they were usually diploid and lacked stabilization of the p53 protein with MSI-H but had a good prognosis after curative cancer surgery. The poorly differentiated colonie adenocarcinomas are mostly located on the left side of the colon, are more infiltrative at the time of diagnosis, and have a somewhat poorer prognosis.

This large cecal mass was tar black grossly. The tumor surface was ulcerated with extensive necrosis and covered with numerous gram-positive and gram-negative rods. Although the tumor was hemorrhagic and the patient was anemic, guaiac test results were negative on 3 occasions. There are normally numerous bacteria present in the colon. Duerden9 reported that all 6 reference strains of Bacteroides species, 36 laboratory isolates conforming to this group, and individual strains of Escherichia coll, Proteus mirabilis, Salmonella Typhimurium, and Clostridium welchii produced a dense black pigment, identified as ferrous sulfide, when grown in cooked meat media that contained cystine and ferrous sulfate.9 It has now been found that most Clostridia (except Clostridia difficile and Clostridia tetani), Proteus vulgaris, Edimrdsiella tarta, Citrobacterfreundii, Salmonella species, and others produce hydrogen sulfide. Hydrogen sulfide combined with ferrous (Fe^sup 2+^) produces insoluble heavy metal sulfides that appear as a black precipitate10: H^sub 2^S + Fe^sup 2+^ [arrow right] Fe^sub 2^(SO^sub 4^)^sub 3^(Fe^sup 3+^) + black precipitate. That is most likely why the ulcerated surface of the tumor was tar black. At the same time, the ferrous iron in the heme became ferric iron. The guaiac test checks for only heme (ferrous iron; Fe^sup 2+^) but not ferric iron (Fe^sup 3+^). This probably explains why 3 guaiac test results were negative. Therefore, if a patient is anemic and the guaiac test result is negative, gastrointestinal hemorrhage still cannot be totally excluded, especially with bleeding from the lower gastrointestinal tract.


1. Jessurun J, Romero-Guadarrama M, Manivel JC. Medullary adenocarcinoma of the colon: clinicopathologic study of 11 cases. Hum Pathol. 1999;30:843-848.

2. Ponz de Leon M, Di Gregorio C. Pathology of colorectal cancer. Dig Liver Dis. 2001:33:372-388.

3. Appleman H. Surgical pathology of the gastrointestinal tract. ASCP Educational Course presented at the Newport Marriott; lune 2-6, 1998; Newport, Rl.

4. Cibbs NM. Undifferentiated carcinoma of the large intestine. Histopathology. 1977; 1:77-84.

5. Lanza G, Gafa R, Matteuzzi M, Santini A. Medullary-type poorly differentiated adenocarcinoma of the large bowel: distinct clinicopathologic entity characterized by microsatellite instability and improved survival. J Clin Oncol. 1999; 17:2429-2438.

6. Dolcetti R, Viel A, Doglioni C, et al. High prevalence of activated intraepithelial cytotoxic T lymphocytes and increased neoplastic cell apoptosis in colorectal carcinomas with microsatellite instability. Am J Kithol. 1999:154:1805-1813.

7. Alexander J, Watanabe T, Wu TT, Rashid A, Li S, Hamilton SR. Histopathological identification of colon cancer with microsatellite instability. Ami Pathol. 2001:158:527-535.

8. Ruschoff J, Dietmaier W, Luttges J, et al. Poorly differentiated colonie adenocarcinoma, medullary type: clinical, phenotypic and molecular characteristics. Am J Pathol. 1997;150:1815-1825.

9. Duerden Bl. Pigment production by Bacteroides species with reference to sub-classification. I Med Microbiol. 1975;8:113-125.

10. Korenman EW, Alien SD, Janda WM, Schreckenberger PC, Winn WC Jr. Color Atlas and Textbook of Diagnostic Microbiology. 5th ed. Baltimore, Md: Lippincott Williams & Wilkins; 1997:187-196.

Lina Wang, MD, MS; Nancy E. Warner, MD; Andy E. Sherrod, MD

Accepted for publication July 21, 2004.

From the Department of Pathology, Charles R. Drew University of Medicine and Science, UCLA School of Medicine, MLK Jr/Drew Medical Center (Dr Wang), and Department of Pathology, University of Southern California, Keck School of Medicine, Morris Comprehensive Cancer Center (Drs Warner and Sherrod), Los Angeles, Calif.

The authors have no relevant financial interest in the products or companies described in this article.

Corresponding author: Lina Wang, MD, MS, Department of Pathology, Charles R. Drew University, 12021 S Wilmington Ave, Los Angeles, CA 90059 (e-mail:

Reprints not available from the authors.

Copyright College of American Pathologists Jan 2005
Provided by ProQuest Information and Learning Company. All rights Reserved

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