Benjazia Elhem, Khalifa Mabrouk, Benabdelkader Atef, Laatiri Adnene, Braham Ahlem, Letaief Amel, Bahri Fethi
Elhem Benjazia, Mabrouk Khalifa, Ahlem Braham, Fethi Bahri, Amel Letaief, Department of Internal Medicine and Infectious disease, University Hospital Farhat Hached, Sousse 4000, Tunisia.
World J Gastrointest Pathophysiol. 2010 Oct 15;1(4):144-6. doi: 10.4291/wjgp.v1.i4.144.
Granulocytic sarcoma is an uncommon and localized extramedullary tumor composed of immature granulocytic cells. It may present in association with acute myeloid leukaemia, myelodysplastic syndrome and chronic myelogenous leukaemia. Granulocytic sarcoma may occur in any anatomical site but involvement of the gastrointestinal tract is rare, especially in the rectum. We report on the case of a 17 year old female who presented with rectal bleeding, abdominal pain and weight loss one mo prior to admission. Rectosigmoidoscopy revealed a rectal polypoid and ulcerated mass. The histological examination of the mass showed granulocytic sarcoma. Bone marrow examination was compatible with acute promyelocytic leukaemia (FAB type M3). This case report is a reminder of this peculiar sign of tumoral syndrome in acute myeloid leukaemia. We also discuss diagnostic methods and analyze the disease course.
粒细胞肉瘤是一种罕见的局限性髓外肿瘤,由未成熟粒细胞组成。它可能与急性髓系白血病、骨髓增生异常综合征和慢性粒细胞白血病相关。粒细胞肉瘤可发生于任何解剖部位,但胃肠道受累罕见,尤其是直肠。我们报告一例17岁女性,入院前1个月出现直肠出血、腹痛和体重减轻。直肠乙状结肠镜检查发现直肠息肉样溃疡肿物。肿物组织学检查显示为粒细胞肉瘤。骨髓检查符合急性早幼粒细胞白血病(FAB分型M3)。本病例报告提醒注意急性髓系白血病中这种特殊的肿瘤综合征表现。我们还讨论了诊断方法并分析了病程。