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

Inês Pestana, Juliana Pedro, Carolina Simões, Carlos Noronha Ferreira, Sara da Mata, Isabel Claro
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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.
经颈静脉肝活检:了解骨髓移植后胆汁淤积性肝炎罕见病因的关键
简介造血干细胞移植(HSCT)与多种并发症有关,如窦性阻塞综合征(SOS)(肝肿大、腹水、黄疸和血小板减少)和移植物抗宿主疾病(GVHD)(主要侵犯皮肤、胃肠道和肝脏)。这些疾病可能会出现重叠的临床表现,因此需要进行鉴别诊断,但它们同时存在的情况非常罕见。病例介绍:一名 29 岁男性急性髓性白血病患者接受了造血干细胞移植。第(D)+20 天,他出现了高胆红素血症、胸腔积液、腹水和疼痛性肝肿大。腹部超声检查提示为 SOS,并开始使用去纤维化药物。D+44日,出现急性皮肤、肠道和肝脏GVHD,经甲基强的松龙治疗后好转。D+132 天,胆汁淤积和腹痛症状加重。MRCP 显示肝内胆管多处狭窄,主胆管不规则。由于肝酶变化加重和临床症状恶化,他被送进了重症监护室。由于严重的高胆红素血症(30 mg/dL)和血小板减少症(30,000 cells/uL)持续存在,他接受了肝血流动力学检查,结果显示肝静脉压力梯度为 10 mm Hg。经颈静脉肝活检发现管状肝胆汁淤积、胆管损伤、局灶性肝细胞坏死,提示为肝脏坏死性炎症,同时还发现小叶中心静脉损伤和小叶中心坏死,可能与 SOS 相吻合。患者开始接受霉酚酸酯治疗,但在 D+195 时死于脓毒性休克。讨论/结论:该病例因其复杂性和罕见的 SOS 和 GVHD 组织学特征并存而引人注目。虽然临床和实验室检查结果可能足以确诊,但必须强调的是,对这些通常伴有严重血小板减少的患者进行肝血流动力学检查和经颈静脉肝活检对于胆汁淤积性肝炎的定性和组织学确诊非常重要,尤其是当病因可能是多因素时。
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