The authors report 2 cases presenting with juvenile fibromatosis of the fingers. The disease was remarkable for its relapses and the presence of intracytoplasmic eosinophilic inclusions. The cause of this original anatomo-clinical entity is discussed. No argument was found in favor of a viral origin.
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Urol Case Rep
January 2025
Department of Urology, Shandong Provincial Third Hospital, Shandong University, Jinan, 250012, China.
To improve the understanding and treatment level of urogenital nerve fibroma by sharing the clinical manifestations, imaging features, and pathological characteristics of a case of urogenital nerve fibroma.The patient was a middle-aged male with initial symptoms of painless gross hematuria, bladder irritation, and pelvic mass. Imaging examination showed a bladder mass, and transurethral bladder tumor resection was performed to reduce the tumor.
View Article and Find Full Text PDFOral Maxillofac Surg
January 2025
Department of Dentistry, State University of Maringá (UEM), Maringá, Brazil.
Background: Hybrid Odontogenic Tumors (HOT) are defined by the presence of two or more independent odontogenic tumors that originate from and affect the same maxillofacial site.
Methods: The present study is the first case report of a mandibular HOT consisting of Ameloblastoma, Calcifying Epithelial Odontogenic Tumor, and Ameloblastic Fibroma.
Case Report: A 37-year-old otherwise healthy male presented with the chief complaint of swelling in the right mandibular body.
Int J Burns Trauma
December 2024
Department of Orthopaedic Surgery, J.N. Medical College, Faculty of Medicine, A.M.U. Aligarh, UP, India.
Chondromyxoid fibroma (CMF) in the foot is a rare condition. We report a case of CMF in a 7-year-old girl, affecting the distal phalanx of the great toe. Radiographs revealed a lytic lesion involving the entire distal phalanx, with destruction of both the medial and lateral cortices, while the articular surfaces remained intact.
View Article and Find Full Text PDFF S Rep
December 2024
Division of Gynecology, Department of Surgery, Boston Children's Hospital, Boston, Massachusetts.
Objective: To characterize the presentation and surgical management of ovarian fibromas among a case series of pediatric and adolescent patients with Gorlin syndrome.
Design: Retrospective case series.
Setting: Tertiary-care hospital.
J Clin Imaging Sci
December 2024
Department of Radiology, Weifang People's Hospital, Weifang, China.
Desmoplastic fibroma (DF) is an uncommon benign bone tumor that typically affects the facial bones, with cerebral cranium involvement being extremely rare. We report a unique case of DF in the parietal bone of a 28-year-old woman, notable for its rapid growth during pregnancy-a phenomenon not previously documented. The imaging features of this case also differ from all but one previously reported case.
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