克罗恩病并发血红蛋白E (HbE)病表现为黑素色伴严重贫血

A. Z. Tanni, D. S. Ahmed, Md Ibrahim Siddique, M. Chowdhury
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摘要

血红蛋白E (HbE)病是一种遗传性常染色体隐性遗传病,表现为轻度贫血和偶尔轻微脾肿大,但通常没有疾病症状,不需要治疗。克罗恩病是一种罕见的炎症性肠病,其复发和缓解过程通常持续数年,涉及胃肠道的任何部分,表现为腹痛、腹泻和体重减轻,在孟加拉国是一种罕见的疾病。我们在此报告一例23岁女性HbE病合并黑素色和严重贫血,后来诊断为克罗恩病并发HbE病。
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Crohn’s Disease Concurrent with Hemoglobin E (HbE) Disease Manifested as Melaena with Severe Anaemia
Hemoglobin E (HbE) disease is an inherited autosomal recessive disorder presented as mild anaemia and occasionally a slightly enlarged spleen but usually do not have disease symptoms and do not require treatment. Crohn’s disease is an uncommon inflammatory bowel disease having relapsing and remitting course usually extending over years involving any part of the gastrointestinal tract presenting as abdominal pain, diarrhea and weight loss, a rare disease in Bangladesh. Here we are presenting a case of 23-year- old female of HbE disease with melaena and severe anaemia who later diagnosed as Crohn’s disease concurrent with HbE disease.
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