Khillare Kishor M, Vaishnav Bhumika, Doshi Nikhil I, Pailla Ruchitha, Wadivkar Aniruddh
General Medicine, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Cureus. 2024 Sep 27;16(9):e70308. doi: 10.7759/cureus.70308. eCollection 2024 Sep.
Hereditary spherocytosis (HS) is a genetic disorder characterized by the presence of spherocytes, which are abnormally shaped red blood cells, leading to hemolytic anemia. While HS is not uncommon in hematology, it can present significant diagnostic and therapeutic challenges in its late stages, particularly when complicated by severe cholestasis. We report a case of a 48-year-old male presenting with jaundice and abdominal pain, initially diagnosed with cholecystolithiasis and moderate splenomegaly. Subsequent investigations confirmed HS through clinical observation and eosin-5'-maleimide (EMA) binding by flow cytometry. The patient exhibited severe jaundice (total bilirubin: 19.58 mg/dL) but no anemia. The complexity of his condition necessitated a multidisciplinary approach involving hematologists and gastroenterologists along with general medicine. This case underscores the importance of considering HS in the differential diagnosis of cholestasis and highlights the need for comprehensive diagnostic strategies to manage such complications effectively.
遗传性球形红细胞增多症(HS)是一种遗传性疾病,其特征是存在球形红细胞,即形状异常的红细胞,可导致溶血性贫血。虽然HS在血液学中并不罕见,但在其晚期可能会带来重大的诊断和治疗挑战,尤其是在并发严重胆汁淤积时。我们报告一例48岁男性,表现为黄疸和腹痛,最初诊断为胆囊结石和中度脾肿大。随后通过临床观察和流式细胞术检测嗜酸性-5'-马来酰亚胺(EMA)结合情况确诊为HS。该患者出现严重黄疸(总胆红素:19.58mg/dL)但无贫血。其病情的复杂性需要血液科医生、胃肠病科医生以及全科医生采取多学科方法。该病例强调了在胆汁淤积的鉴别诊断中考虑HS的重要性,并突出了有效管理此类并发症所需综合诊断策略的必要性。