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Case Report: Patent ductus arteriosus with tuberous sclerosis complex.
Front Cardiovasc Med
July 2024
Department of ICU, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.
Article Synopsis
- A 33-year-old patient with a long-standing patent ductus arteriosus (PDA) was examined, revealing various fibromas and a shagreen patch, leading to a genetic test that confirmed Tuberous Sclerosis Type 2 (TSC2).
- The patient underwent additional imaging studies, which validated the presence of PDA, a condition more commonly associated with TSC in children rather than adults.
- The article aims to investigate the genetic relationship between TSC and PDA through a review of existing literature.
Giant cell angiofibroma of gingiva in tuberous sclerosis complex: a case report and literature review.
Diagn Pathol
March 2024
Department of Oral Pathology, School of Dentistry, Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju, 61186, Republic of Korea.
Background: Tuberous sclerosis complex (TSC) is a rare, complex genetic disorder characterized by hamartomas and neoplastic lesions in various organ systems. With the development of radiology and gene testing, the diagnostic criteria for TSC were updated in 2012 at the International Consensus Conference. Intraoral fibromas have long been associated with TSC.
View Article and Find Full Text PDFTuberous sclerosis complex: A clinical diagnosis in Ethiopian patients.
Medicine (Baltimore)
February 2024
Department of Radiology, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Article Synopsis
- - Tuberous sclerosis complex (TSC) is a rare genetic disorder causing nonmalignant growths in various organs, with delayed diagnosis often resulting from a lack of physician familiarity.
- - Two patients, a 27-year-old man with kidney issues and a 28-year-old woman with seizures, were diagnosed with TSC through established diagnostic criteria and exhibited various skin lesions.
- - Both patients were advised to receive ongoing care: the male was referred to a chronic illness clinic, while the female was scheduled for dermatological treatment for her facial lesions.
Giant Cell Angiofibroma in the Buccal Mucosa - A Rising Entity?
Anticancer Res
April 2023
Department of Oral and Maxillofacial Surgery, Army Hospital Hamburg, Hamburg, Germany.
Background: Tumors of the oral cavity must be differentiated into benign and malignant. Rare tumors must also be considered throughout the differential diagnosis when dealing with pathologic changes in the oral mucosa. Examples of rare benign tumors within the oral cavity are solitary fibrous tumors (SFTs).
View Article and Find Full Text PDFAngiofibroma of the Mandible: Report of a Rare Case.
Case Rep Dent
April 2022
Dammam regional lab and blood bank, Saudi Arabia.
Angiofibroma is an uncommon, highly vascular benign lesion that occurs in the head and neck region, typically arising in the nasopharyngeal area, potentially with a locally aggressive course. Angiofibroma with a primary intraoral presentation is extremely rare; few case reports have been published in the literature, with only three cases of angiofibroma in the mandible published to date. In this case, a 37-year-old man presented with swelling at the right mandible and underwent enucleation of the lesion under general anesthesia.
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