Kimura H, Nasu K, Sakai C, Shiga Y, Miyamoto E, Shintaku M, Wakatsuki S, Tominaga K, Abe M, Maruyama Y
Internal Medicine, Hobara Central Hospital, Fukushima, Japan.
Leuk Lymphoma. 1998 Sep;31(1-2):217-24. doi: 10.3109/10428199809057601.
We report three patients with histiocytic sarcoma of the spleen associated with severe hypoalbuminemia, hypo gamma-globulinemia and thrombocytopenia. After the clinical diagnosis of splenic tumor of unknown origin was made, all three patients underwent splenectomy. The histiocytic origin of the tumor was confirmed histopathologically and immunohistochemically using a panel of antibodies. In contrast to malignant histiocytosis (MH), which typically reveals severe generalized clinical manifestations and a rapidly fatal course caused by the disseminated proliferation of neoplastic histiocytes, these patients were asymptomatic or showed only mild clinical symptoms for a long period of time until the recurrence was detected by which time the tumor cells had already spread to other organs. All three cases were characteristically associated with hypoalbuminemia, hypo gamma-globulinemia and thrombocytopenia, which returned to normal after splenectomy. Splenic histiocytic sarcoma with the features described here may represent a unique clinical entity, distinct from MH.
我们报告了三例脾组织细胞肉瘤患者,他们均伴有严重低白蛋白血症、低γ球蛋白血症和血小板减少症。在临床诊断为不明来源的脾肿瘤后,所有三名患者均接受了脾切除术。通过一组抗体进行组织病理学和免疫组织化学检查,证实了肿瘤的组织细胞起源。与恶性组织细胞增多症(MH)不同,MH通常表现出严重的全身性临床表现,且由于肿瘤性组织细胞的播散性增殖而导致病程迅速致命,而这些患者在很长一段时间内无症状或仅表现出轻微的临床症状,直到检测到复发时肿瘤细胞已经扩散到其他器官。所有三例均典型地伴有低白蛋白血症、低γ球蛋白血症和血小板减少症,脾切除术后这些指标恢复正常。具有此处所述特征的脾组织细胞肉瘤可能代表一种独特的临床实体,有别于MH。