Results 41 to 50 of about 259,450 (135)
UEG Week 2022 Poster Presentations
United European Gastroenterology Journal, Volume 10, Issue S8, Page 473-1092, October 2022.
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
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Large Uterine Angiolipoleiomyoma Masquerading as an Ovarian Tumor: A Case Report
Angiolipoleiomyoma (ALLM) is a rare benign mesenchymal tumor that primarily arises in the skin and kidney, and less frequently in the uterus. The present case may represent the largest reported uterine mass described as ALLM. We present a case of a 52‐year‐old woman with abdominal fullness and an irregular menstrual cycle having a large cystic ...
Prabineshwor Prasad Lekhak +7 more
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Epithelioid angiomyolipoma of the kidney
Epithelioid angiomyolipoma is a recently recognized variant of angiomyolipoma, which is characterized by the presence of polygonal cells with densely eosinophilic cytoplasm and varying degrees of nuclear atypia. Only a relatively small number of cases of
Oner, U +4 more
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Advances in the Diagnosis, Treatment, and Management of Liver Nodules: A Comprehensive Review
Liver nodules commonly occur due to various causes, some of which are malignant or may undergo malignant transformation, leading to disease progression or delayed detection in clinical practice. The widespread use of imaging methods has increased the detection rate of liver nodules. Furthermore, precision medicine techniques and artificial intelligence
Chang Gao, Dongyang Chen, Youpeng Chen
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Epithelioid Angiomyolipoma: A Case Report
Epithelioid angiomyolipoma is a recently recognized tumor entity. We report a case of epithelioid angiomyolipoma of the kidney that occurred in a 70-year-old female. The patient presented with massive abdominal hemorrhage and shock. There was no history
Tuncer, C +7 more
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Epithelioid hepatic angiomyolipoma (Epi-HAML) is a rare benign mesenchymal tumor with malignant potential. Most of Epi-HAML contains no or only a minimal amount of adipose tissue and poses a diagnostic challenge.
Ruo-Kun Li, Meng-Su Zeng, Jin-Wei Qiang
doaj +1 more source
ABSTRACT 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 renal disease (ESRD).
Changlin Wei +5 more
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Incidental Primary Angiomyolipoma of Ovary: A Rare Case Report and Literature Review
ABSTRACT Primary angiomyolipomas of the ovary which are not associated with genetical systemic diseases, particularly tuberous sclerosis, are extremely rare and are more likely to pose diagnostic challenges. This tumor, particularly of epithelioid variant, is more likely to be malignant and can carry a high possibility of metastasizing.
James J. Yahaya +3 more
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Hepatic angiomyolipoma: mutation analysis and immunohistochemical pitfalls in diagnosis [PDF]
AIMS: Hepatic angiomyolipoma (AML) often shows epithelioid morphology with inconspicuous fat. Epithelioid component can mimic hepatocellular adenoma (HCA) or carcinoma (HCC).
Kakar, Sanjay +13 more
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