腹膜后肥大细胞肉瘤并发全身性肥大细胞增多症和未披露的相关血液学肿瘤:1例报告。

IF 1.9 Q3 PATHOLOGY Clinical Pathology Pub Date : 2022-09-13 eCollection Date: 2022-01-01 DOI:10.1177/2632010X221123539
Ing Chen, Jia-Bin Liao, Jung-Chia Lin, Pin-Pen Hsieh, Ming-Yun Hsieh
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引用次数: 0

摘要

肥大细胞增多症是一种罕见的疾病,影响儿童和成人的功能缺陷肥大细胞聚集在身体组织。世界卫生组织(WHO)将肥大细胞增多症分为皮肤肥大细胞增多症、全身肥大细胞增多症(SM)和肥大细胞肉瘤(MCS)。我们在此报告一例腹膜后MCS并发系统性肥大细胞增多症和未披露的相关血液学肿瘤(sm -未披露的AHN)。MCS和SM的诊断是在对腹膜后肿块、淋巴结和卵巢进行第二次活检后做出的,该疾病进展迅速,除了腹痛外,还伴有不明原因的反复潮红、心悸和休克。核型和血象资料也怀疑为克隆性髓系肿瘤。不幸的是,病人很快就死于这种疾病。除了这个独特的病例外,我们还回顾了文献中先前报道的SM合并MCS的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Mast Cell Sarcoma of the Retroperitoneum With Concurrent Systemic Mastocytosis and an Undisclosed Associated Hematologic Neoplasm: A Case Report.

Mastocytosis is a rare disorder affecting both children and adults by gathering of functionally defective mast cells in the body's tissues. The World Health Organization (WHO) classified mastocytosis into cutaneous mastocytosis, systemic mastocytosis (SM), and mast cell sarcoma (MCS). We hereby present a case of retroperitoneal MCS with concurrent systemic mastocytosis and an undisclosed associated hematological neoplasm (SM-undisclosed AHN). The diagnosis of MCS and SM was made after the second biopsy over retroperitoneal mass, lymph node, and ovary for rapidly progressive disease with the presentation of unexplained recurrent flushing, palpitation, and shock, in addition to abdominal pain. A clonal myeloid neoplasm was also suspected by the karyotype and hemogram data. Unfortunately, the patient succumbed to the disease quickly. Apart from this unique case, the previously reported cases of SM with MCS in the literature were also reviewed.

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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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