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经颈静脉肝活检:骨髓移植后胆汁淤积性肝炎罕见病因的关键

Transjugular Liver Biopsy: The Key to a Rare Etiology of Cholestatic Hepatitis after Bone Marrow Transplantation.

作者信息

Pestana Inês, Pedro Juliana, Simões Carolina, Ferreira Carlos Noronha, da Mata Sara, Claro Isabel

机构信息

Serviço de Gastrenterologia, Hospital Amato Lusitano ULSCB, Castelo Branco, Portugal.

Serviço de Gastrenterologia e Hepatologia, Centro Hospitalar Universitário Lisboa Norte, Lisboa, Portugal.

出版信息

GE Port J Gastroenterol. 2024 Mar 14;31(6):437-442. doi: 10.1159/000536535. eCollection 2024 Dec.

Abstract

INTRODUCTION

Hematopoietic stem cell transplantation (HSCT) is associated with multiple complications, such as sinusoidal obstruction syndrome (SOS) (hepatomegaly, ascites, jaundice, and thrombocytopenia) and graft-versus-host disease (GVHD) (with the skin, gastrointestinal tract, and liver being the main targets). These entities may present overlapping clinical findings, being considered differential diagnoses, but their coexistence is rare.

CASE PRESENTATION

A 29-year-old male with acute myeloid leukemia underwent HSCT. On day (D)+20, he developed hyperbilirubinemia, pleural effusion, ascites, and painful hepatomegaly. Abdominal ultrasound was suggestive of SOS, and defibrotide was initiated. On D+44, acute cutaneous, intestinal, and hepatic GVHD developed which improved after treatment with methylprednisolone. On D+132, there was worsening cholestasis and abdominal pain. MRCP revealed strictures in several segments of the intrahepatic bile ducts and irregularity of the main bile duct. Due to aggravation of liver enzyme changes and clinical worsening, he was admitted to the Intensive Care Unit. Due to persistence of severe hyperbilirubinemia (30 mg/dL) and thrombocytopenia (30,000 cell/uL), he underwent a hepatic hemodynamic study which revealed a hepatic venous pressure gradient of 10 mm Hg. The transjugular liver biopsy revealed canalicular hepatic cholestasis, bile duct injury, and focal hepatocellular necrosis suggestive of GVHD as well as injury to centrilobular veins and centrilobular necrosis compatible with possible SOS. Mycophenolate mofetil was started, but on D+195, the patient died of septic shock.

DISCUSSION/CONCLUSION: This case is notable for its complexity and for demonstrating the rare coexistence of histological features of SOS and GVHD. Although the clinical and laboratory findings may be sufficient for the diagnosis, it is important to highlight the importance of liver hemodynamic study and transjugular liver biopsy in these patients who often have severe thrombocytopenia, for the characterization and histological confirmation of cholestatic hepatitis, especially when the etiology may be multifactorial.

摘要

引言

造血干细胞移植(HSCT)与多种并发症相关,如肝窦阻塞综合征(SOS)(肝肿大、腹水、黄疸和血小板减少)和移植物抗宿主病(GVHD)(主要累及皮肤、胃肠道和肝脏)。这些病症可能存在重叠的临床症状,需进行鉴别诊断,但其同时存在的情况较为罕见。

病例介绍

一名29岁的急性髓系白血病男性患者接受了HSCT。在移植后第(D)+20天,他出现了高胆红素血症、胸腔积液、腹水和肝肿大伴疼痛。腹部超声提示为SOS,遂开始使用去纤苷治疗。在D+44天,出现了急性皮肤、肠道和肝脏GVHD,经甲泼尼龙治疗后有所改善。在D+132天,胆汁淤积和腹痛加重。磁共振胰胆管造影(MRCP)显示肝内胆管多个节段狭窄以及主胆管不规则。由于肝酶变化加剧和临床症状恶化,他被收入重症监护病房。由于严重高胆红素血症(30mg/dL)和血小板减少(30,000细胞/微升)持续存在,他接受了肝脏血流动力学研究,结果显示肝静脉压力梯度为10mmHg。经颈静脉肝活检显示胆小管胆汁淤积、胆管损伤以及提示GVHD的局灶性肝细胞坏死,同时伴有中央小叶静脉损伤和与可能的SOS相符的中央小叶坏死。开始使用霉酚酸酯,但在D+195天,患者死于感染性休克。

讨论/结论:该病例因其复杂性以及罕见地同时出现SOS和GVHD的组织学特征而值得关注。尽管临床和实验室检查结果可能足以做出诊断,但对于这些常伴有严重血小板减少的患者,强调肝脏血流动力学研究和经颈静脉肝活检对于胆汁淤积性肝炎的特征描述和组织学确诊的重要性非常重要,尤其是当病因可能是多因素时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7862/11614426/375ba2086da1/pjg-2024-0031-0006-536535_F01.jpg

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