Results 81 to 90 of about 6,672 (205)
Angiofibroma en un individuo de época medieval (s. XII-XIII) [PDF]
, 2011 X Congreso Nacional de Paleopatología.
Campillo Valero, D., Garcia Guixé, E.
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The nasopharyngeal angiofibroma
Clinical Radiology, 1967 Twelve cases of angiofibromata of the nasopharynx are described. Ten patients were adolescent males, 2 were females. The aetiology is discussed but in this series endocrine dysfunction was not obvious. The technique of irradiation used is described and the results presented. Irradiation appears to act by initiating thrombosis and fibrosis in the tumour
openaire +3 more sources
American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.ABSTRACT Cardiac rhabdomyomas are often the presenting sign of tuberous sclerosis complex (TSC). Prior reports have shown that maternal sirolimus treatment can reduce rhabdomyomas. We used maternal sirolimus to reverse hydrops fetalis due to a massive cardiac rhabdomyoma in a twin gestation.
David M. Ritter +6 more
wiley +1 more source
Juvenile Nasopharyngeal Angiofibroma
Otolaryngologic Clinics of North America, 2011 Juvenile nasopharyngeal angiofibromas (JNAs) are rare, benign, highly vascular, locally aggressive tumors that primarily affect male adolescents. Historical treatment of these neoplasms has been primarily surgical. In the past decade, endoscopic resection of JNAs has become a viable and promising surgical treatment option. Endoscopic resection has many
Angela, Blount +2 more
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Clinical Case Reports, Volume 13, Issue 10, October 2025.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
wiley +1 more source
Juvenile nasopharyngeal angiofibroma
Journal of Oral and Maxillofacial Pathology, 2016 Juvenile nasopharyngeal angiofibroma (JNA) is a rare benign tumor arising predominantly in the nasopharynx of adolescent males. It is an aggressive neoplasm and shows a propensity for destructive local spread often extending to the base of the skull and into the cranium.
Makhasana, Jashika Adil Shroff +3 more
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Extranasopharyngeal Angiofibroma: A Diagnostic Dilemma
Philippine Journal of Otolaryngology Head and Neck Surgery, 2018 Objective: To report two cases of extranasopharyngeal angiofibroma, highlighting the diagnostic challenges involved. Methods: Design: Case Report Setting: Tertiary Teaching Hospital and Medical School
Nitin Gupta +4 more
doaj +1 more source
A rare form of discoid lupus erythematosus as a rosacea and angiofibroma: A case report
Clinical Case Reports, 2020 The rare presentation of DLE can be rosacea‐/angiofibroma‐like lesions which should be considered in patients with red‐pink to skin‐color papules with flushing and photosensitivity.
Fatemeh Mokhtari, Zakiye Ganjei
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Orbital causes of incomitant strabismus [PDF]
, 2015 Strabismus may result from abnormal innervation, structure, or function of the extraocular muscles. Abnormalities of the orbital bones or masses within the orbit may also cause strabismus due to indirect effects on the extraocular muscles.
Lueder, Gregg T
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Facial Pain as the Initial Presentation of Rhabdomyosarcoma: A Case Report
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Spindle cell/sclerosing rhabdomyosarcoma (RMS) is an uncommon and aggressive neoplasm, especially in adults. This case details a 35‐year‐old male with a 4‐year history of persistent idiopathic facial pain (PIFP), first misdiagnosed owing to the lack of definitive clinical or radiologic evidence.
Najmeh Anbiaee +4 more
wiley +1 more source