结缔组织增生小圆细胞瘤(DSRCT) 1例报告及文献复习

A. Morshed, F. Afroz, C. Galib, S. Islam, K. Hasina, A. Ghosh
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引用次数: 1

摘要

结缔组织增生小圆细胞瘤(DSRCT)是一种罕见的病理实体,最常见于儿科和青少年男孩的腹膜腔。它经常出现在晚期,通常预后较差。有时在诊断时可能累及肝脏。我们提出一个不寻常的病例DSRCT谁是目前肿块在下腹,疼痛,肝肿大和轻度腹水。这种肿瘤的特征是小的未分化细胞巢,显示上皮、间充质和神经分化的免疫组织化学证据。本例患者的肿瘤具有DSRCT的组织学特征,由小而圆的细胞组成,细胞核深染,细胞质稀少。由于诊断困难重重,我们最终通过开放活检和免疫组织化学进行诊断。目前患者正在接受多药化疗(修改后的p6方案)。一种罕见肿瘤的诊断和治疗需要高度的怀疑和及时的干预。DOI: http://dx.doi.org/10.3329/jpsb.v2i2.19552
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Desmoplastic Small Round Cell Tumour (DSRCT) - A Case Report and Review of Literature
Desmoplastic small round cell tumor (DSRCT) is a rare pathologic entity that most frequently affects the peritoneal cavity and presents in pediatric and adolescent boys. It often presents at an advanced stage and has a generally poor prognosis. Sometimes it may involve liver at diagnosis. We present an unusual case of DSRCT who was present with mass in lower abdomen, pain, hepatomegaly and mild ascites. This tumor is characterized by nests of small undifferentiated cells that show immunohistochemical evidence of epithelial, mesenchymal and neural differentiation. In our patient histologicaly tumor had the characteristic features of DSRCT and were composed of small round cells with hyperchromatic nuclei and scanty cytoplasm. With various difficulties in diagnosis we ultimately reached at diagnosis by open biopsy and immunohistochemistry. Now patient is on multidrug chemotherapy (modified p6 protocol). Diagnosis and management of a rare tumor needs high level of suspicion and in time intervention. DOI: http://dx.doi.org/10.3329/jpsb.v2i2.19552
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