Evidence map›Paper›PMID 35658280›Full record

ArticleInternational journal of surgery case reports2022

Giant hepatic angiomyolipoma presenting with severe anemia: A surgical case report and review of literature.

Cong Long Nguyen, Ham Hoi Nguyen, Tuan Hiep Luong, Nghe Tinh Nguyen, Van Khang Le, Truong Khanh Vu

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Article in International journal of surgery case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 49% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Cong Long NguyenDepartment of Gastroenterology & Hepatology, Bach Mai Hospital, Ha Noi, Viet Nam; School of Medicine and Pharmacy, Vietnam National University, Hanoi, Viet Nam.
Ham Hoi NguyenDepartment of Gastrointestinal and Hepato-Pancreato-Biliary Surgery, Bach Mai Hospital, Hanoi, Viet Nam.
Tuan Hiep LuongDepartment of Surgery, Hanoi Medical University, Viet Nam. Electronic address: hiep1995hsgs@gmail.com.
Nghe Tinh NguyenDepartment of Gastroenterology & Hepatology, Bach Mai Hospital, Ha Noi, Viet Nam.
Van Khang LeRadiology Center, Bach Mai Hospital, Hanoi, Viet Nam.
Truong Khanh VuTam Anh Hospital, Hanoi, Viet Nam; School of Medicine and Pharmacy, Vietnam National University, Hanoi, Viet Nam.
Bạch Mai Hospital · VNVietnam National University, Hanoi · VNHanoi Medical University · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAngiomyolipoma (AML) is a solid benign neoplasm with mesenchymal features. The clinical signs and symptoms of hepatic angiomyolipoma are nonspecific, and treatment strategy is variable. PRESENTATION: A 35-years-old male patient has admitted to the hospital with symptoms of severe anemia. Abdominal multi-slice computed tomography (MSCT) and Gadoxetic acid (GA)-enhanced magnetic resonance imaging (MRI) revealed a heterogeneous 23 × 17 cm-in-sized tumor with heterogeneous enhancement and increased angiogenesis. Percutaneous hepatic biopsy was proceeded and in immunohistochemistry, tumor cells responded positively to the HMB-45, SMA, and Glutamine stains, the CD-34 stain was positive for blood vessels as well as Ki-67 sporadically positive, but the Heppar1, S-100, CK stains reacted negative. The final pathologic result was consistent with the primary hepatic angiomyolipoma. The final surgical management was extended right hepatectomy with ligation of the right hepatic artery (RHA) and vein (RHV), as well as the middle hepatic vein (MHV), one month after portal embolization as well as to enlarge the remnant liver volume. DISCUSSION: A hepatic angiomyolipoma (HAML) primary origin is relatively rare, the clinical manifestations are variable and non-specific. Histological examination and immunohistochemistry staining are considered as the gold standard for HAML diagnosis. HAML are commonly expressed benign behaviors, but HAML cases with malignant behaviors were reported in a cumulative incidence. Radical surgery must be still the most effective and major treatment approach.

conclusionThe present case being the first case with initial syndrome of severe anemia accounted in the English literature. Giant angiomyolipoma is composed of blood vessels and could lead to extensive internal tumoral hemorrhage. We here present a report of this case with had primary hepatic angiomyolipoma with clinical picture of severe anemia.

Indexed as

AngiomyolipomaCase reportHepaticSevere Anemia

Identifiers

PMID35658280
PMCPMC9171536
OpenAlexW4224315671

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.