Results 51 to 60 of about 2,097 (120)
Low‐grade oncocytic tumor (LOT) of the kidney is a rare, indolent neoplasm within the spectrum of eosinophilic renal tumors. It typically presents as a small, solitary mass and is associated with molecular alterations in TSC1, TSC2, or MTOR. We describe a 72‐year‐old male with a history of pancreatic neuroendocrine tumor, gastrointestinal stromal tumor,
Ilham Putra +4 more
wiley +1 more source
Introduction. Angiomyolipoma is a common benign renal tumor. It is associated with Tuberous Sclerosis Complex (TSC) in 20% of patients. Angiomyolipomas are classically multiple, bilateral, and growing; they may lead to complications such as Wunderlich ...
Adrien Riviere +2 more
doaj +1 more source
Perivascular Epithelioid Cell Neoplasm of the Lung: A Patient Case Report
Perivascular epithelioid cell tumors (PEComa) are a family of tumors characterized by epithelioid cells and are often found in perivascular spaces. Cases originating in the lungs are highly uncommon. We discuss the case of a pulmonary PEComa found in a 71‐year‐old male who had two instances of lung cancer 4 years prior.
Calista Sha +4 more
wiley +1 more source
Two variants of renal angiomyolipoma (AML)—classic and epithelioid—have been described. Although the epithelioid variant has been reported to demonstrate an aggressive clinical behavior, classic AML is usually benign.
Cristina Fox +6 more
doaj +1 more source
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
wiley +1 more source
Epithelioid Angiomyolipoma of Liver with an Inflammatory Component: A Case Report
Angiomyolipomas (AMLs) are benign mesenchymal tumors seen in kidneys in association with tuberous sclerosis. They are uncommon in liver. Angiomyolipomas of liver show great histological diversity and various types and patterns are described.
Jyothi C. R. +3 more
doaj +1 more source
Introduction Lymphangioleiomyomatosis (LAM) is a rare, progressive, multisystem disease primarily affecting women of reproductive age. It is characterized by the abnormal proliferation of smooth muscle‐like LAM cells that infiltrate the lungs, lymphatics, and kidneys.
Shiva Ebrahimi +4 more
wiley +1 more source
Recurrent Pneumothorax Revealing Lymphangioleiomyomatosis in a Young Woman: A Case Report
ABSTRACT Lymphangioleiomyomatosis (LAM) should be considered in young women presenting with recurrent pneumothorax. Early diagnosis through high‐resolution computed tomography(HRCT)and histopathological analysis is essential for timely management and improved patient outcomes.
Qihang Zhang +3 more
wiley +1 more source
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
wiley +1 more source
Clinical behavior and management of three types of renal angiomyolipomas
Objectives: To analyze and present the demography, clinical behavior, especially the risk factors of tumor hemorrhage and management of sporadic angiomyolipoma (SAML), tuberous sclerosis complex associated angiomyolipoma (TSCAML) and epithelioid ...
Kun-Han Lee +6 more
doaj +1 more source

