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卵巢粒细胞肉瘤。一例不寻常的病例报告。

Granulocytic sarcoma of the ovary. An unusual case presentation.

作者信息

Magliocco A M, Demetrick D J, Jones A R, Kossakowska A E

机构信息

Department of Pathology, Foothills Hospital, Calgary, Alberta, Canada.

出版信息

Arch Pathol Lab Med. 1991 Aug;115(8):830-4.

PMID:1863196
Abstract

We report an unusual occurrence of granulocytic sarcoma presenting as an ovarian mass in a 46-year-old woman with a history of dysplastic nevus syndrome. During workup of the ovarian mass, the diagnosis of acute myelogenous leukemia was made. A fine-needle aspirate of the ovarian mass showed granulocytic sarcoma. The patient died of complications of the acute leukemia a short time later. A postmortem examination was performed, which confirmed the nature of the ovarian mass as a granulocytic sarcoma. Material was obtained for flow cytometry, immunohistochemical and histochemical studies, and electron microscopy. Ploidy analysis of the tumor showed it to be diploid with an S phase of 4.8% and a G2 + M ratio of 0.5%. To our knowledge, there is only one previous report of a primary ovarian presentation of granulocytic sarcoma, and only four cases in which granulocytic sarcoma was diagnosed by fine-needle aspiration cytology. The association between dysplastic nevus syndrome and acute myeloid leukemia in this case is discussed with reference to a review of the metachronous association between melanoma and leukemia as described in the literature.

摘要

我们报告了一例罕见的粒细胞肉瘤,表现为一名46岁患有发育异常痣综合征病史的女性的卵巢肿块。在对该卵巢肿块进行检查期间,确诊为急性髓细胞白血病。对卵巢肿块进行细针穿刺抽吸显示为粒细胞肉瘤。患者不久后死于急性白血病并发症。进行了尸检,证实卵巢肿块的性质为粒细胞肉瘤。获取了材料用于流式细胞术、免疫组织化学和组织化学研究以及电子显微镜检查。肿瘤的倍性分析显示其为二倍体,S期为4.8%,G2 + M比率为0.5%。据我们所知,之前仅有一篇关于粒细胞肉瘤原发性卵巢表现的报告,且仅有4例通过细针穿刺细胞学诊断为粒细胞肉瘤。结合文献中描述的黑色素瘤与白血病的异时性关联综述,讨论了该病例中发育异常痣综合征与急性髓细胞白血病之间的关联。

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