Small Round Cell Tumors

Author(s):  
B. Mackay ◽  
D. Garza

The term "small round cell tumor" is used to designate a heterogenous group of neoplasms that have in common the fact that they are composed of small round, polygonal, or occasionally ovoid cells, compactly grouped with little or no evidence of architectural organization. Identification of tumors within this group by light microscopy can be difficult and is often not possible. Selection of a specific diagnosis by the pathologist is frequently influenced by the clinical behavior and location of the tumor, and by the age of the patient. For example, tumors with this morphology occurring in young children are usually assumed to be rhabdomyosarcoma, neuroblastoma, Ewing's sarcoma, or lymphoma.By studying these neoplasms with the electron microscope and correlating the findings with the light microscopic and clinical data, it is possible to reach a specific diagnosis in most cases. Each tumor possesses distinctive ultrastructural features that serve to identify the cell type.

2006 ◽  
Vol 130 (5) ◽  
pp. 728-732 ◽  
Author(s):  
Fuju Chang

Abstract Desmoplastic small round cell tumor (DSRCT) is a recently recognized clinicopathologic entity that has a predilection for adolescent males and usually affects the abdominal cavity. Due to its uncommon nature, many pathologists lack experience with this tumor. The literature regarding DSRCT is reviewed with special attention to its histologic and cytologic diagnosis. Morphologic features of DSRCT and its immunohistochemical and cytogenetic profile are summarized and differential diagnosis with other small round cell tumors is discussed. As observed by both histologic and cytologic examinations, small round blue cells and fibrosclerotic stroma are the striking morphologic features of DSRCT. The typical immunohistochemical profile is characterized by coexpression of epithelial, mesenchymal, myogenic, and neural markers. Cytogenetically, this tumor harbors a specific karyotypic abnormality, namely t(11;22)(p13;q12). These features distinguish DSRCT from other members of the family of small round cell tumors.


2018 ◽  
Vol 27 (3) ◽  
pp. 236-243 ◽  
Author(s):  
Alyaa Al-Ibraheemi ◽  
Cory Broehm ◽  
Munir R. Tanas ◽  
Andrew E. Horvai ◽  
Brian P. Rubin ◽  
...  

Objectives. Desmoplastic small round cell tumor (DSRCT) is an aggressive round cell sarcoma that arises in the abdominal cavity/pelvis of young males. We sought to expand its clinicopathologic spectrum. Methods. Cases of DSRCT presenting in patients >30 years of age or tumors arising outside of the abdominal cavity/pelvis were retrieved. Results. Thirty-four cases were identified. Sixteen tumors arose at atypical sites (head/neck, intracranial, thigh, axilla/shoulder, inguinal/paratesticular, intraosseous, and uterine corpus). The remaining 18 patients were older than 30 years, and their tumors involved the abdomen or pelvis. The majority of cases showed areas with classic histology, while 6 cases exhibited solid growth and 5 showed macronodular architecture. Cytologic appearance included round cell, rhabdoid, epithelioid, and small cell. Conclusion. DSRCT may arise at nonabdominal locations in both pediatric and adult populations, as well as intra-abdominally in older adults, and these tumors exhibit high rates of metastasis and morbidity.


2021 ◽  
Vol 23 (1) ◽  
pp. 128-132
Author(s):  
Amir G. Abdullaev ◽  
Nikolay A. Kozlov ◽  
Nikolay K. Schakhpazyan ◽  
Anna V. Tsigankova

Solitary fibrous tumor and desmoplastic small round cell tumor are primary peritoneal malignant tumors. Despite their morphological differences, these diseases are united by low morbidity, the lack of pathogenic symptoms, similar radiological signs, and scant knowledge of prognostic factors. Considering the low morbidity, reliable differential diagnostic signs have not been established at present, which greatly complicates the timely formulation of the diagnosis. On the contrary, cases of choosing the wrong treatment tactics and the lack of a unified management algorithm are increasingly being identified. Radiation and instrumental diagnostic methods such as computed tomography, magnetic resonance imaging, laparoscopy are crucial in determining the extent of the tumor, it is necessary to take into account the biological characteristics of the tumor (morphological type), which affect the nature of tumor growth. With a solitary fibrous tumor and a desmoplastic small-round cell tumor, the computed tomography picture is characterized by the presence of isolated nodular formations in any part of the abdominal cavity, which can also be accompanied by a large omentum, ascites, an increase in retroperitoneal lymph nodes, and distant metastasis to the lungs and bones is possible. In general, the main task of diagnosing a primary peritoneal neoplasm is to take sufficient quality biological material, with the leading role in the diagnosis being given to histological and immunohistochemical studies. On the other hand, the independent experience of many clinics does not exceed single surveillance. This information does not allow doctors to confidently navigate the problem; accordingly, there is a need for multicenter and, possibly, prospective, randomized scientific research in order to develop a unified algorithm for managing patients with primary peritoneal tumors. The approaches to the treatment of these tumors are currently not standardized and not well studied due to the rarity of the pathology. According to the available information, the treatment of desmoplastic small round cell tumors is based on multimodal therapy, including systemic chemotherapy and surgery, and possibly radiation therapy. Traditional treatment algorithms for this pathology include the surgical stage and systemic or intracavitary chemotherapy, while the treatment sequence may be different and depends primarily on the prevalence of the disease. For solitary fibrous tumor, surgical treatment, by contrast, is the method of choice. Thus, when choosing a treatment strategy for a primary peritoneal tumor, it is first of all necessary to take into account the morphological type of the tumor and rely on known data on the benefits of a particular method. In this article, we tried to present modern information on the diagnosis and treatment of rare forms of primary peritoneal tumors.


2017 ◽  
Vol 12 ◽  
Author(s):  
Alessandro Giuseppe Fois ◽  
Pietro Pirina ◽  
Antonella Arcadu ◽  
Francesca Becciu ◽  
Sandra Manca ◽  
...  

Desmoplastic small round cell tumor of the pleura is a rare malignancy, with only a few cases reported in the scientific literature. The aim of the present review is to discuss the demographic, pathological, clinical, and therapeutic features of this rare tumor. English-language articles published since 1989, when the first case of desmoplastic small round cell tumor of the pleura was described, were retrieved, and fifteen cases included in fourteen articles were revised. The mean age of the patients was 25.5 years, out of them 60% were males. Chest pain, pleural effusion, and dyspnea were the most common clinical manifestations, while chest roentgenogram and computed tomography were the imaging techniques most commonly used. Surgical biopsy was employed in 80% of the cases for diagnosis. A multidisciplinary approach consisting in a combination of surgery with chemotherapy and radiation therapy was adopted in most cases. Only two patients (13.3%) were alive at 3 years from diagnosis, reflecting the aggressiveness of the disease, and the poor outcomes of the treatments currently available. Desmoplastic small round cell tumors of the pleura are extremely aggressive and challenging to diagnose, because of their rarity and unspecific demographic, clinical, and radiological features. An in-depth knowledge of such features is necessary for the optimal management of patients with this rare malignancy.


2007 ◽  
Vol 10 (4) ◽  
pp. 320-324 ◽  
Author(s):  
Sophie Collardeau-Frachon ◽  
Dominique Ranchère-Vince ◽  
Olivier Delattre ◽  
Stelly Hoarau ◽  
Philippe Thiesse ◽  
...  

We report a case of desmoplastic small round cell tumor (DSRCT) arising in the kidney of a 14-year-old female. The subject presented with gross hematuria. Medical imaging uncovered a left renal mass without regional or metastatic extension. The tumor showed morphological, immunohistochemical, and molecular features of DSRCT. Immunostaining revealed polyphenotypic differentiation. Molecular analysis detected the fusion transcript resulting from the t(11;22)(p13;q12) reciprocal translocation, which characterized this neoplasm. Desmoplastic small round cell tumor is a rare, aggressive neoplasm that mainly affects young males and that usually presents with widespread abdominal serosal involvement. This unusual localization should lead one to consider this tumor in the differential diagnosis of small blue round cell tumors of the kidney.


2020 ◽  
Vol 53 (3) ◽  
pp. 177-182
Author(s):  
Atsushi Kihara ◽  
Kazuya Takahashi ◽  
Ayataka Ishikawa ◽  
Yusuke Amano ◽  
Daisuke Matsubara ◽  
...  

2015 ◽  
Vol 45 (9) ◽  
pp. 1308-1315 ◽  
Author(s):  
Austin Ostermeier ◽  
M. Beth McCarville ◽  
Fariba Navid ◽  
Scott E. Snyder ◽  
Barry L. Shulkin

ORL ◽  
2021 ◽  
pp. 1-6
Author(s):  
Qingjiao Li ◽  
Xiaolu Yuan

Desmoplastic small round cell tumor (DSRCT) is a rare and aggressively malignant tumor mostly occurring in the abdominal and pelvic cavity of young patients. However, few cases had been reported concerning DSRCT occurring in the head and neck region. We presented a rare case of DSRCT of the right submandibular in a 25-year-old man. MRI revealed a 3 × 2-cm solid nodule located in the right submandibular, and physical examination showed no other occupying lesion elsewhere. Histologically, the tumor was composed of various-sized small round cell nests, embedded in an abundant desmoplastic stroma. Immunohistochemically, the tumor cells were typically positive for epithelial (CK and EMA), mesenchymal (vimentin and desmin), and neuroendocrine (CD56, NSE, Syn, and CgA) markers, but negative for WT1. Fluorescence in situ hybridization revealed the presence of a break apart involving the <i>Ewing sarcoma</i> (<i>EWS</i>) gene. The patient received chemotherapy and radiotherapy and relapsed after 19 months of follow-up. DSRCT of the submandibular gland is rare, and the diagnosis of this tumor in an uncommon location relies on the histomorphology, immunophenotype, and <i>EWS</i> gene translocation detection. Differential diagnosis including primary salivary gland tumors and the other small round cell tumors needs to be excluded.


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