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A rare cause of variceal bleeding

机译:曲张静脉出血的罕见原因

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BACKGROUND: Agnogenic myeloid metaplasia (AMM) is a clonal stem cell disease, which is characterized by myelofibrosis, osteosclerosis and pancytopenia. Affected patients frequently develop portal hypertension secondary to extramedullary hematopoiesis, which rarely becomes clinically relevant. CASE REPORT: We here report on a 63-year-old patient with a first presentation of variceal bleeding. The patient was diagnosed with portal hypertension and due to marked splenomegaly, liver cirrhosis was suspected. Subsequently, an extramedullary hematopoiesis and AMM could be diagnosed. The variceal bleeding was initially treated endoscopically. The patient has received cytoreductive therapy and a splenorenal shunt, which has led to remission and long-term survival. CONCLUSION: Agnogenic myeloid metaplasia is a rare cause of portal hypertension and may present with variceal bleeding. Clinicians should be aware of this rare cause of portal hypertension, as treatment of the underlying disease with cytoreductive therapy and appropriate management of portal hypertension may lead to long-term survival.
机译:背景:血管源性髓样化生(AMM)是一种克隆性干细胞疾病,其特征是骨髓纤维化,骨硬化和全血细胞减少。受影响的患者经常会因髓外造血继发发展为门脉高压,这在临床上几乎没有意义。病例报告:我们在这里报告了一名63岁的患者,该患者首次出现静脉曲张性出血。该患者被诊断为门静脉高压症,由于脾肿大,怀疑有肝硬化。随后,可以诊断出髓外造血和AMM。内镜治疗静脉曲张破裂出血。该患者已接受细胞减灭疗法和脾肾分流术,导致缓解和长期生存。结论:血管源性淀粉样化生是门脉高压的罕见原因,可能伴有静脉曲张破裂出血。临床医生应意识到这种罕见的门脉高压病因,因为通过细胞减灭疗法治疗基础疾病和适当管理门脉高压病可能会导致长期生存。

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