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脾脏原发性非淋巴网状恶性肿瘤。

Primary nonlymphoreticular malignant neoplasms of the spleen.

作者信息

Wick M R, Scheithauer B W, Smith S L, Beart R W

出版信息

Am J Surg Pathol. 1982 Apr;6(3):229-42. doi: 10.1097/00000478-198204000-00005.

Abstract

Primary sarcomas of the spleen are exceedingly uncommon neoplasms, approximately 90 substantiated cases having been reported. We report on six cases of primary splenic angiosarcoma and three cases of primary malignant fibrous histiocytoma of the spleen which have been seen at the Mayo Clinic during the last 51 years. In one of the cases of splenic angiosarcoma, the lesion was manifested by spontaneous rupture and hemoperitoneum; interestingly, two cases of splenic malignant fibrous histiocytoma were of the inflammatory type and showed corresponding clinical features of a systemic nature. Five patients with angiosarcoma of the spleen died of metastatic tumor within 3 years after diagnosis; one patient with splenic malignant fibrous histiocytoma is alive with metastasis 11/2 years after splenectomy. One case of splenic angiosarcoma and two of malignant fibrous histiocytoma of the spleen have been diagnosed only recently. All three patients are alive and currently tumor-free, from 3 to 7 months after diagnosis.

摘要

脾脏原发性肉瘤是极其罕见的肿瘤,据报道约有90例确诊病例。我们报告了梅奥诊所过去51年间所见的6例脾脏原发性血管肉瘤和3例脾脏原发性恶性纤维组织细胞瘤。在1例脾脏血管肉瘤病例中,病变表现为自发性破裂和腹腔积血;有趣的是,2例脾脏恶性纤维组织细胞瘤为炎症型,表现出相应的全身性临床特征。5例脾脏血管肉瘤患者在诊断后3年内死于转移性肿瘤;1例脾脏恶性纤维组织细胞瘤患者在脾切除术后1年半出现转移,仍存活。1例脾脏血管肉瘤和2例脾脏恶性纤维组织细胞瘤最近才被诊断出来。所有3例患者均存活,目前诊断后3至7个月无肿瘤。

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