Fatal gastrointestinal bleeding as the primary manifestation of granulocytic sarcoma in a patient with myelodysblastic syndrome.

H A Saleh, G Khatib
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Abstract

Granulocytic sarcoma (GS), or chloroma, is a rare extramedullary tumor composed of immature myeloid cells. It most commonly involves bone, soft tissue, lymph nodes and skin and develops during the course of or preceding myelogenous leukemia (ML). Involvement of other organs has been rarely reported including ovary, uterus and cervix, lung and the gastrointestinal tract; however, GS presenting as upper and lower gastrointestinal (GI) bleeding from ulcerated gastric mass and concurrent bleeding vaginal mass is an unusual rare manifestation of GS. We describe a case of GS in a 70 year old black woman who presented with a bleeding "lump" in the vaginal wall and suffered fatal GI bleeding from an ulcerated gastric lesion. She was diagnosed with myelodysblastic syndrome a few months earlier. From the review of the available English literature, this is a unique presentation of GS. It is important to include this entity in the differential diagnosis when encountering GI bleeding particularly in a patient previously diagnosed with myeloid leukemia or preleukemia. The importance of Naphthol Chloracetate Esterase (NCAE) stain and lysozyme immunoperoxidase stain in establishing the diagnosis is breifly discussed.

致死性胃肠道出血是骨髓增生异常综合征患者粒细胞肉瘤的主要表现。
粒细胞肉瘤是一种罕见的髓外肿瘤,由未成熟的髓样细胞组成。它最常累及骨骼、软组织、淋巴结和皮肤,并在髓性白血病(ML)的过程中或之前发生。很少有报道累及其他器官,包括卵巢、子宫、子宫颈、肺和胃肠道;然而,GS表现为上、下胃肠道(GI)溃疡性胃肿块出血并并发阴道肿块出血是GS的一种罕见表现。我们描述了一个70岁的黑人妇女的GS病例,她表现为阴道壁出血的“肿块”,并因胃病变溃疡而发生致命的胃肠道出血。几个月前,她被诊断出患有骨髓增生异常综合征。从现有的英文文献来看,这是一种独特的GS表现。当遇到消化道出血时,特别是在先前诊断为髓性白血病或白血病前期的患者中,将这一实体纳入鉴别诊断是很重要的。本文简要讨论了萘酚氯乙酸酯酶(NCAE)染色和溶菌酶免疫过氧化物酶染色在该病诊断中的重要性。
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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