小肠上皮样血管肉瘤表现为难治性胃肠道出血:一种罕见的肿瘤,诊断困难,预后差

C. Onyenekwu, Reena Singh, J. A. Miller, M. Mostafa
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摘要

胃肠道血管肉瘤是一种罕见的血管源性恶性肿瘤。通常,这种肿瘤是由于头颈部和软组织等其他部位的转移而发生的。当作为肠道原发肿瘤发生时,由于其非特异性临床表现,再加上其浸润性特征,可能在没有明显病变的情况下发生,常规胃肠道干预使该实体面临诊断困境。从尸检和外科病例的发现,简要回顾其诊断特点和相关文献进行了讨论。方法:我们提出一个73岁的男性与胃肠道出血的历史最近发作谁被转介到我们的设施持续出血。他接受了内窥镜检查,但没有发现出血的明显来源,随后在我们的医院接受了结肠切除术,并因持续的胃肠道出血反复输血。他最终被转移到临终关怀医院,并在演讲后不久去世。进行了完整的尸检。结果:腹腔内无血,肠腔内无血。小肠黏膜有三个出血性结节。组织学上,结节显示中至大上皮样血管形成性肿瘤细胞浸润穿过小肠壁并延伸到网膜。大体和组织学检查以及免疫组织化学染色的结果与上皮样血管肉瘤一致。结论:原发性肠上皮样血管肉瘤是一种罕见的侵袭性肿瘤,其诊断具有挑战性。虽然罕见,但在难治性消化道出血患者中需要考虑这种诊断。由于其形态与其他良性和恶性肿瘤重叠,在组织学检查中使用辅助测试是准确诊断的关键。
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Epithelioid angiosarcoma of the small intestine presenting with intractable gastrointestinal bleeding: An uncommon tumor with diagnostic challenge and poor prognosis
Introduction: Angiosarcoma of the gastrointestinal tract is a rare, aggressive malignant neoplasm of vascular origin. Commonly, this tumor occurs due to metastases from other sites like the head and neck region and the soft tissue. When occurring as a primary tumor of the intestines, this entity poses a diagnostic dilemma due to its non-specific clinical presentation, coupled to its infiltrative features that may occur without an obvious lesion amenable to routine gastrointestinal interventions. The findings from an autopsy and surgical case with a brief review of its diagnostic features and relevant literature are discussed.Methods: We present a 73-year-old male with a history of a recent onset of gastrointestinal bleeding who was referred to our facility for persisting bleeding. He underwent endoscopy without an identifiable source of bleeding and subsequently received a colectomy at our facility, with repeated blood transfusions for persisting gastrointestinal bleeding. He was eventually transitioned to hospice and died shortly after presentation. A complete autopsy was performed.Results: There was anasarca with hemoperitoneum and intestinal intraluminal blood. Present in the small intestinal mucosa were three hemorrhagic nodules. Histologically, the nodules demonstrated medium to large epithelioid vasoformative neoplastic cells infiltrating through the wall of the small intestine and extending to the omentum. The findings from the gross and histology examination, as well as the immunohistochemical stains were consistent with an epithelioid angiosarcoma.Conclusion: Primary epithelioid angiosarcoma of the intestine is an uncommon aggressive tumor that poses a diagnostic challenge. Although rare, this diagnosis needs to be considered in patients with intractable gastrointestinal bleeding. Due to its morphologic overlap with other benign and malignant neoplasms, the use of ancillary testing during histologic examination is key in arriving at an accurate diagnosis.
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