Results 41 to 50 of about 252,515 (144)
More than Pus – Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess
Hepatic angiomyolipomas (AML) are rare mesenchymal tumours of which the epithelioid type is a rare type with malignant potential. We report a case of primary hepatic epithelioid angiomyolipoma masquerading as liver abscess.
Wen Hao Justin Leong +2 more
doaj +1 more source
Interventional oncology in children: Where are we now?
Abstract Paediatric Interventional Oncology (IO) lags behind adult IO due to a scarcity of specific outcome data. The suboptimal way to evolve this field is relying heavily on adult experiences. The distinct tumour types prevalent in children, such as extracranial germ cell tumours, sarcomas, and neuroblastoma, differ strongly from those found in ...
Premal Amrishkumar Patel +1 more
wiley +1 more source
Wunderlich's syndrome with hepatic angiomyolipoma in tuberous sclerosis [PDF]
We present a patient of tuberous sclerosis complex with bilateral renal angiomyolipoma and hepatic angiomyolipoma with spontaneous retroperitoneal hemorrhage from right angiomyolipoma (Wunderlich′s syndrome). Nephron preserving approach was tried but
Mongha, R +4 more
core
ABSTRACT Background and Aim Accurate diagnosis of focal liver lesions (FLLs) is crucial for determining the appropriate treatment strategies. Although percutaneous liver biopsy (PLB) is the standard diagnostic procedure, it has limitations, particularly for difficult‐to‐access lesions.
Kei Yane +9 more
wiley +1 more source
Spontaneous haemorrhage of an adrenal angiomyolipoma: case report [PDF]
Background Angiomyolipomas are rare mesenchymal tumours arising from the perivascular epithelioid cells consisting of variable amounts of adipose, thick-walled blood vessels and smooth muscle cells.
Seshadri Sriprasad +4 more
core +1 more source
Mitochondrial DNA Depletion Syndrome 1 (MTDPS1)—A Novel Cause of Premature Ovarian Insufficiency
We describe a woman with MNGIE due to a novel homozygous TYMP nonsense variant and propose MNGIE as the cause of her premature ovarian insufficiency—a rarely reported association—highlighting the need to consider mitochondrial disease in unexplained POI, especially in atypical, consanguineous presentations. ABSTRACT Mitochondrial DNA depletion syndrome
Michael Matheou +3 more
wiley +1 more source
Femoral PEComa Treated With Combined Surgery and Radiotherapy: A Case Report
ABSTRACT Perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal tumor, and primary involvement of the bone is exceptionally uncommon. In this report, a case of malignant PEComa arising from the femur in an elderly patient is described.
Yanluqi He +4 more
wiley +1 more source
Renal Angiomyolipoma in a Young Woman With Tuberous Sclerosis: A Case Report
ABSTRACT Tuberous sclerosis is a rare autosomal dominant genetic disorder caused by mutations in tumor suppressor genes (TSC1/2), leading to hamartomas in multiple organs. Renal angiomyolipomas are often asymptomatic but can cause mass effects or bleeding if they enlarge, requiring treatment.
Donald Dominick Lema +7 more
wiley +1 more source
Hepatic Angiomyolipoma : a case report [PDF]
We experienced a rare case of hepatic angiomyolipoma (AML). A 66-year old Japanese female presented inhomogeneous echogenic lesion in the lateral segment of the liver on ultrasonography.
Nakashima, Akira +7 more
core
Nitrofurantoin, a first‐line antibiotic, works effectively for treating uncomplicated urinary tract infections, but it can cause severe liver damage. In the setting of concurrent supplement use, distinguishing what caused liver damage is challenging. A 57‐year‐old woman who had nonalcoholic fatty liver disease developed sudden jaundice after finishing ...
Edwin Mendoza +8 more
wiley +1 more source

