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伴有严重腹腔内出血的肝细胞腺瘤,与潜在的凝血障碍相关:一例报告。

Hepatocellular adenomas with severe intra-abdominal bleeding, related to an underlying coagulation disorder: a case report.

机构信息

Erasmus MC Transplant Institute, Department of Surgery, Division of Hepatobiliary and Transplantation Surgery, University Medical Center Rotterdam, Office RG-220, Dr. Molewaterplein 40, 3015 GD, Rotterdam, the Netherlands.

Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.

出版信息

J Med Case Rep. 2024 Aug 13;18(1):367. doi: 10.1186/s13256-024-04709-7.

Abstract

BACKGROUND

Hepatocellular adenoma is a rare benign liver tumor. Typically, hepatocellular adenomas are solitary and are found in young women who use estrogen-containing contraceptives. The occurrence of multiple hepatocellular adenoma has been linked to higher body mass index, and as the prevalence of overweight increases, multiple hepatocellular adenomas are seen more often. An hepatocellular adenoma does not always necessitate treatment, as they can regress under conservative strategies. In incidental cases, an adenoma presents owing to bleeding, which is mostly self-limiting. If it is not, embolization of hepatic involved vessels is indicated.

CASE PRESENTATION

In this case report, we discuss a 42-year old Caucasian woman with multiple hepatocellular bleeds, treated by multiple endovascular procedures. After the first embolization of an adenoma in the right liver lobe, a second bleed occurred in the left lobe, necessitating additional endovascular intervention. During admittance, treatment was complicated by pulmonary embolism and a pneumonia. During follow-up, our patient was diagnosed with antiphospholipid syndrome.

CONCLUSION

Hepatocellular adenoma is a rare diagnosis that requires centralized expertise. This particular case illustrates the complexity of treatment strategies for associated intra-abdominal bleeding and possible complications. Although liver adenoma is often an incidental finding, it can also result in significant morbidity. Centralization of treatment leads to expertise in managing complex treatment strategies.

摘要

背景

肝细胞腺瘤是一种罕见的良性肝肿瘤。通常,肝细胞腺瘤是单发的,发生在使用含雌激素避孕药的年轻女性中。多发性肝细胞腺瘤的发生与较高的体重指数有关,随着超重的流行,多发性肝细胞腺瘤越来越常见。肝细胞腺瘤并不总是需要治疗,因为它们可以在保守策略下消退。在偶发情况下,由于出血而出现腺瘤,这种出血大多是自限性的。如果不是,建议栓塞肝内受累血管。

病例介绍

在本病例报告中,我们讨论了一位 42 岁的白人女性,她因多发性肝细胞出血接受了多次血管内治疗。在右肝叶的腺瘤第一次栓塞后,左叶再次出血,需要进行额外的血管内介入治疗。在住院期间,患者出现肺栓塞和肺炎等并发症。在随访期间,我们的患者被诊断为抗磷脂综合征。

结论

肝细胞腺瘤是一种罕见的诊断,需要集中的专业知识。本例说明了与腹腔内出血相关的治疗策略的复杂性和可能的并发症。虽然肝腺瘤通常是偶然发现的,但它也可能导致严重的发病率。治疗的集中化可导致对复杂治疗策略的管理专业知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/11321172/61c8b8f2c23d/13256_2024_4709_Fig1_HTML.jpg

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