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Vestibular Schwannoma in a paediatric case-A rare entity.
J Oral Maxillofac Pathol
July 2024
Department of Oral Medicine and Radiology, Maulana Azad Institute of Dental Sciences, New Delhi, India.
Article Synopsis
- * A notable case involved a 13-year-old girl with a Schwannoma located in the vestibular mucosa, which is an unusual site for this type of tumor.
- * Histological examination revealed characteristic features of Antoni type A tissue, and the patient remained free of recurrence six months post-surgery, highlighting the rarity and uniqueness of this case.
Colocolic intussusception due to lipoma in an adolescent with refractory anal fissure; case report and literature review.
Int J Surg Case Rep
June 2024
Department of General Surgery, Imam Hosein Medical and Educational Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address:
Article Synopsis
- Intussusception is rare in older patients, making it hard to diagnose, and it usually appears differently in adults compared to children, often leading to delayed diagnosis.
- The article discusses a case of a 13-year-old boy with chronic anal fissure and constipation, where an MRI unexpectedly revealed a colocolic intussusception.
- The case highlights the need for healthcare professionals to consider intussusception as a possible diagnosis in teenagers, even when symptoms seem nonspecific.
Spinal Dysraphism Presenting as Neuropathic Ulcers: A Case Report of a Delayed Diagnosis.
Case Rep Dermatol
September 2023
Consultant Pediatric Dermatology, Department of Dermatology, King Abdulaziz Hospital, Makkah, Kingdom of Saudi Arabia.
Spinal dysraphism (SD) refers to the abnormal fusion of dorsal midline structures during embryogenesis. It encompasses a variety of congenital spinal defects, ranging from an overt defect in which neural tissue is exposed with no overlying skin (open SD) such as myelomeningoceles to skin-covered malformations (closed or occult SD). A 13-year-old boy presented with recurrent multiple painless ulcers and erosions over the tips of the toes, mainly involving the right foot with hemorrhagic crusts for 5 years.
View Article and Find Full Text PDFBipartite craniopharyngeal canal with a lipoma and cephalocele: a previously unreported entity.
Acta Neurochir (Wien)
February 2019
Department of Imaging Sciences and Interventional Radiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Room no 318, Srishty building, SCTIMST Staff Quarters, Poondi Road, Kumarapuram Junction, Medical college (P.O), Trivandrum, Kerala, 695011, India.
A 13-year-old male child was evaluated for headache and visual deterioration; he underwent routine MRI imaging which revealed a large craniopharyngeal canal, divided by an abnormal bony septum giving a bipartite appearance of the canal, with a lipoma and cephalocele on either side of the septum. The child had undergone a previous surgery for cleft palate repair at the age of 7. The child had normal pituitary function inspite of nonvisualization of pituitary gland in MRI.
View Article and Find Full Text PDFLingual Chondrolipoma in a Dog.
J Comp Pathol
July 2017
Department of Veterinary Pathology, School of Veterinary Medicine, Nippon Veterinary and Life Science University, Tokyo, Japan.
A 13-year-old female Yorkshire terrier was presented with difficulty swallowing because of a lingual mass, which had grown to a size of 0.8 × 0.8 × 0.
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