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Pregnancy-Related Eccrine Angiomatous Hamartoma: Case Report.
Cureus
January 2024
Dermatopathology, Clinica CES, Medellín, COL.
Eccrine angiomatous hamartoma is rare, slow-growing, and benign neoplasm that is diagnosed based on clinical characteristics and histological findings. It usually presents as a solitary nodule on the extremities and may arise at birth or in childhood. Although it is usually asymptomatic, in some cases it can cause pain and hyperhidrosis.
View Article and Find Full Text PDFEccrine Angiomatous Hamartoma With Arteriovenous Malformation: A Rare Entity Re-Explored.
Cureus
March 2022
Pathology and Laboratory Medicine, King Faisal Hospital, Makkah, SAU.
Eccrine angiomatous hamartoma (EAH) is a rare, benign, slow-growing cutaneous lesion characterized by hamartomatous proliferation of the eccrine glands and vascular structures. It usually arises in early childhood; however, cases in adults have also been reported. It is diagnosed based on the clinical features of the lesion as well as the histopathological findings of the excised tissue.
View Article and Find Full Text PDFHistopathological and Immunohistochemical Evaluation of Meningiomas with Reference to Proliferative Markers p53 and Ki-67.
J Clin Diagn Res
January 2016
Professor, Department of Pathology, SVIMS , Tirupati, Andhra Pradesh, India .
Introduction: Meningiomas are slow growing primary central nervous system (CNS) tumours attached to the duramater, which arise from the meningothelial cells of the arachnoid. Grading of meningioma based on histological findings assisted with supplementary immunohistochemical studies, predicts the prognosis of meningioma with good precision.
Aim: To evaluate proliferative markers and correlate with various histological subtypes and grade.
Slow-growing angiomatous lesions on the limbs.
Cleve Clin J Med
February 2014
Department of Dermatology, Valencia University General Hospital, Valencia, Spain.
Sylvian fissure lipoma with angiomatous component and associated brain malformation: A case report.
Iran J Neurol
November 2013
Resident, Department of Radiology, Indira Gandhi Medical College and Hospital, Shimla, Himachal Pradesh, India.
Article Synopsis
- - Intracranial lipomas are rare congenital tumors, making up about 0.1 to 1.7% of intracranial tumors, often found at the midline or along the sylvian fissures.
- - Seizures are the most common symptom if the lipomas cause any issues, while these tumors generally grow slowly and have a positive prognosis.
- - A case is presented of a 25-year-old man where CT and MRI scans showed a lesion in the right sylvian fissure, indicating a lipoma with abnormal blood vessels and associated cortical dysplasia.
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