Results 1 to 10 of about 252,515 (144)

A case of ruptured hepatic angiomyolipoma in a young male [PDF]

open access: yesClinical and Molecular Hepatology, 2017
A 31-year-old male visited a local hospital due to sudden-onset severe abdominal pain. Abdominal computed tomography revealed a solid cystic mass with a size of approximately 12 cm and exhibiting both hemorrhage and fluid collection in the pelvic cavity.
Sun Hwa Kim   +5 more
doaj   +4 more sources

Contrast-enhanced ultrasound features of hepatic angiomyolipoma: comparison with AFP-negative and non-viral hepatocellular carcinoma [PDF]

open access: yesUltrasound International Open
Purpose This study aimed to compare contrast-enhanced ultrasound (CEUS) features of hepatic angiomyolipoma (HAML) and challenging cases of HCC, mainly those with no hepatitis infection but also with
Yafang Zhang   +7 more
doaj   +3 more sources

Delayed TSC Diagnosis Presenting as End‐Stage Renal Disease With Renal and Hepatic Angiomyolipoma: Case Report and Review [PDF]

open access: yesClinical Case Reports
Tuberous sclerosis complex (TSC) is a rare and complex autosomal dominant disease. Many patients with TSC may remain undiagnosed for years due to its widespread and heterogeneous clinical presentation, with only 1% of TSC patients developing end‐stage ...
Changlin Wei   +5 more
doaj   +3 more sources

Transcatheter arterial embolization followed by laparoscopic anatomic hepatectomy for spontaneous rupture of a giant hepatic angiomyolipoma: a case report [PDF]

open access: yesFrontiers in Surgery, 2023
Hepatic angiomyolipoma is a rare and possibly cancerous mesenchymal tumor that consists of three components: blood vessels, smooth muscle cells, and adipose tissue.
Jianjun Wang   +7 more
doaj   +2 more sources

Insights into hepatic angiomyolipoma: A case report highlighting scannographic findings [PDF]

open access: yesRadiology Case Reports
Hepatic angiomyolipoma (HAML) is a rare, benign tumor characterized by a mixture of fat, smooth muscle, and blood vessels. We present the case of a 37-year-old male with a history of tuberous sclerosis complex who underwent a CT scan to evaluate ...
Fatima Zohra EL Yaagoubi, MD   +3 more
doaj   +2 more sources

Primary hepatic neuroendocrine tumor with multiple intrahepatic metastases and concurrent hepatic angiomyolipoma: a case report and review of the literature [PDF]

open access: yesJournal of Medical Case Reports
Background Primary hepatic neuroendocrine tumor is extremely rare, and hepatic angiomyolipoma is also a rare benign tumor of the liver with malignant biological behavior.
Yu-cen Shao   +3 more
doaj   +2 more sources

Laparoscopic hepatectomy for hepatic angiomyolipoma with preoperative diagnosis of other malignancy: a report of 2 cases [PDF]

open access: yesSurgical Case Reports, 2021
Background Hepatic angiomyolipoma (HAML) is a rare liver tumor, and hepatectomy is the only effective treatment. Due to the difficulty of correct diagnosis of HAML before surgery by image studies, more than 36.6% of reported HAMLs are misdiagnosed as ...
Yoh Asahi   +11 more
doaj   +2 more sources

Case of Hepatic Angiomyolipoma: An Unusual Hepatic Lesion with a Review of Diagnostic and Management Challenges [PDF]

open access: yesThe Korean Journal of Gastroenterology
Hepatic angiomyolipoma (HAML) is a rare, benign mesenchymal tumor with varying proportions of adipose tissue, smooth muscle, and blood vessels in the liver. Often asymptomatic, HAML is usually discovered incidentally during imaging.
Bushra Kurban   +3 more
doaj   +2 more sources

Mapping the Tissue Architecture and Endothelial‐PEC Network in HAML Using Single‐Cell and Spatial Transcriptomics [PDF]

open access: yesCancer Sci
Spatial multi‐omics mapping of hepatic angiomyolipoma reveals that PEComas tightly co‐localize with endothelial cells, which drive autophagic flux in adjacent tumor cells via a paracrine PDGFD–PDGFRB–Ras axis, establishing a compensatory survival network that operates in parallel to canonical TSC–mTOR defects.
Liu X   +9 more
europepmc   +2 more sources

Clinicopathological features and diagnostic challenges of hepatic epithelioid angiomyolipoma: a retrospective analysis of 27 cases [PDF]

open access: yesFrontiers in Medicine
BackgroundHepatic epithelioid angiomyolipoma, a rare mesenchymal tumor, poses significant diagnostic challenges due to its rarity and non-specific presentation.
Erming Cai   +4 more
doaj   +2 more sources

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