Ischemic colitis in a known sickle cell disease patient

A. Dambatta
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Abstract

Patients affected with sickle cell disease (SCD) suffer from recurrent vascular occlusions that lead to ischemia and distal tissue infarction in multiple organs. These vascular occlusions manifest as sickle cell pain crises. Abdominal pain is common in sickle cell pain crises. It is attributed to vasoocclusion or infarction in the mesenteric vasculature. Progression to significant ischemic damage of the intestine is rare in sickle cell disease. The objective was to show the rare case of ischemic colitis in SCD patient. The patient’s images (plain abdominal x rays and barium enema images) and case file were reviewed and summarized. The subject matter of ischemic colitis in a known SCD was reviewed in the literature. The index case was discussed and compared with literature. We report an 18-year-old known SCD patient diagnosed since childhood but not regular on medication and follow up. The patient presented to SCD clinic of Aminu Kano Teaching Hospital (AKTH), Kano with 2-year history of recurrent blood stained and watery stool associated with abdominal pain and low-grade fever. There was history of easy fatigability and multiple blood transfusions in the past. Other systemic reviews were unremarkable. This man is the only sickle cell anemic child among 9 other siblings of the family, and on presentation, a second-year student of a junior secondary school. Examination revealed a stunted young man, mild pale with a tinge of jaundice. Abdominal examination revealed hepatomegaly 4 cm below the costal margin. The spleen was not enlarged. Other systemic reviews were unremarkable. Latest hemoglobin was 5.7 g/dL. Renal and the liver function tests were normal. Stool microscopy did not isolate ova, cyst or protozoa. Barium enema was then requested and showed loss of haustration and cobblestone appearance involving the entire colon. Fine mucosal granulations were also noted in the rectum. Diagnosis of colitis most probably ischemic was made. The patient was commenced on analgesics and antibiotics including azithromycin and metronidazole and made significant improvement. Ischemic colitis in SCD may still be encountered in practice despite its rarity.
1例镰状细胞病患者的缺血性结肠炎
镰状细胞病(SCD)患者反复发生血管闭塞,导致多器官缺血和远端组织梗死。这些血管闭塞表现为镰状细胞痛危象。腹痛是常见的镰状细胞痛危象。它可归因于肠系膜血管的血管闭塞或梗塞。在镰状细胞病中,进展到显著的肠缺血性损伤是罕见的。目的是显示罕见的病例缺血性结肠炎在SCD患者。回顾和总结患者的影像(腹部x线平片和钡餐灌肠片)和病例档案。在一个已知的SCD缺血性结肠炎的主题是回顾在文献。对指标病例进行了讨论,并与文献进行了比较。我们报告一名18岁的SCD患者,自童年诊断,但不定期药物治疗和随访。患者就诊于卡诺Aminu Kano教学医院(AKTH) SCD诊所,卡诺有2年复发性血染和水样便病史,伴有腹痛和低烧。既往有易疲劳及多次输血史。其他的系统评价也不引人注目。这名男子是家中9个兄弟姐妹中唯一患有镰状细胞性贫血的孩子,他是一名初中二年级的学生。检查显示是一个身材矮小的年轻人,脸色苍白,带点黄疸。腹部检查显示肝在肋缘下4cm处肿大。脾脏未肿大。其他的系统评价也不引人注目。最新血红蛋白5.7 g/dL。肾功能和肝功能检查正常。粪便显微镜未检出卵、囊肿或原生动物。随后要求进行钡灌肠,结果显示整个结肠失去排空和鹅卵石样外观。直肠也可见细小的粘膜颗粒。结肠炎诊断为缺血性结肠炎。患者开始使用止痛药和抗生素,包括阿奇霉素和甲硝唑,并取得显著改善。SCD的缺血性结肠炎尽管罕见,但在实践中仍可能遇到。
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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