Unique Variant of Zieve Syndrome With a Normal Reticulocyte Count.

Apurva Vedire, Steven Imburgio, Harshavardhan Sanekommu, Rushi Patel, Haley Johnson, Sobaan Taj, Mohammad Hossain
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Abstract

Zieve syndrome is a rare diagnosis seen in patients with chronic alcohol use which consists of a distinct clinical triad of hyperlipidemia, hemolytic anemia, and jaundice. Patients typically have an elevated reticulocyte count due to the hemolytic nature of the anemia. We present the case of a 44-year-old female who was discovered to have an unusual variant of Zieve syndrome with a normal reticulocyte count, which was believed to be due to suppression of bone marrow from excessive alcohol consumption. She was treated with steroids and complete alcohol cessation, with remarkable improvement on subsequent follow-up. An exhaustive literature review of 31 documented cases of Zieve syndrome was conducted to better understand the clinical presentation and overall prognosis of these patients. This case report and literature review aimed to improve patient outcomes through increased recognition of this underrecognized syndrome.

网织红细胞计数正常的Zieve综合征的独特变体。
Zieve综合征是一种罕见的诊断,见于慢性酒精使用患者,它由高脂血症、溶血性贫血和黄疸的独特临床三联症组成。由于贫血的溶血性,患者通常有网状红细胞计数升高。我们提出的情况下,44岁的女性谁被发现有一个不寻常的Zieve综合征变异与正常的网织红细胞计数,这被认为是由于过度饮酒抑制骨髓。她接受类固醇治疗并完全戒酒,在随后的随访中有显著改善。为了更好地了解这些患者的临床表现和整体预后,我们对31例Zieve综合征的文献进行了详尽的复习。本病例报告和文献综述旨在通过提高对这种未被充分认识的综合征的认识来改善患者的预后。
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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