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Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome.
Turk J Pediatr
May 2024
Division of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Türkiye.
Background: Hyaline fibromatosis syndrome is a rare autosomal recessive disorder caused by ANTXR2 pathogenic variants. The disorder is characterized by the deposition of amorphous hyaline material in connective tissues. The hallmarks of the disease are joint contractures, generalized skin stiffness, hyperpigmented papules over extensor surfaces of joints, fleshy perianal masses, severe diarrhea, and gingival hypertrophy.
View Article and Find Full Text PDFHemorrhoidal disease: Epidemiological study and analysis of predictive factors for surgical management.
J Visc Surg
June 2024
Institut Léopold-Bellan, Service de Proctologie médicochirurgicale, Hôpital Saint-Joseph, 185, rue Raymond-Losserand, 75014 Paris, France.
Introduction: There are very few French studies on hemorrhoidal disease and its management.
Patients And Methods: Prospective single-center study from July to December 2021 including 472 patients.
Results: Bleeding, prolapse and pain were the main reasons for consultation.
Acyclovir-Resistant Anogenital Herpes Simplex Virus in an HIV Patient With Pseudoepitheliomatous Hyperplasia Resembling Squamous Cell Carcinoma.
HCA Healthc J Med
August 2022
ProPath, Dallas, TX.
Background: Herpes simplex virus (HSV) is a common infection. However, it may present atypically when patients are immunocompromised, such as with slowly expanding, long-lasting ulcerative or hypertrophic lesions. The histopathologic finding of pseudoepitheliomatous hyperplasia (PEH) can occur in a variety of situations where there is chronic inflammation and can be seen in patients with chronic HSV.
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