Results 1 to 10 of about 2,505 (153)

Gastric Choristoma of the Oropharynx [PDF]

open access: yesClinical and Experimental Otorhinolaryngology, 2009
Heterotopic gastric mucosa tissue is also called gastric choristoma, and this type of lesion can be found anywhere in the alimentary tract. However, gastric choristoma in the pharynx is very rare; only 10 cases of pharyngeal gastric choristoma have been ...
Azzie   +14 more
core   +5 more sources

Osseous choristoma: Report of a case on the palate and a literature review. [PDF]

open access: yesClin Case Rep, 2023
Microscopic sections of the lesion revealed hard tissue composed of osseous tissue surrounded by cartilage, which was covered with parakeratnized squamous epithelium. Key Clinical Message Osseous choristoma is a rare entity, mainly found on the posterior tongue. It is described as a nodular or exophytic lesion with firm to hard consistency.
Shamloo N, Modanloo K, Khaleghi A.
europepmc   +2 more sources

Dorsal duplication of paw pads in the four limbs of a cat [PDF]

open access: yesVeterinary Dermatology, Volume 34, Issue 4, Page 359-362, August 2023., 2023
An approximately one-year-old intact male domestic short hair cat was presented with plantigrade stance and dorsally duplicated paw pads in all limbs covered by hyperkeratotic material.
Ginel, Pedro J.   +3 more
core   +2 more sources

Young Female With Gingival Lesion of Intraoral Osseous Choristoma: A Rare Case Report. [PDF]

open access: yesCase Rep Dent
Choristoma is a mass of tissue with normal histology similar to a part of the body that is different from the one in which it is located. It differs from the hamartomatous group of pathology which is normal tissue, but disorganized, found in an abnormal location.
Alhakim AK, Moussa SA, Halboub E.
europepmc   +2 more sources

An Atypical Presentation of Osseous Choristoma in a 63-Year-Old Male: A Lesion Beyond the Common Demographic and Anatomical Norms. [PDF]

open access: yesCureus
Osseous choristomas, characterized by ectopic bone, are rare and typically found in the head and neck, particularly on the tongue. This report describes a unique case of an osseous choristoma in a 63-year-old male with an unusual posterior tongue ...
Aplanalp CJ   +4 more
europepmc   +3 more sources

Cartilaginous Choristoma of the Oral Cavity: A Rare Presentation in the Nasopharynx. [PDF]

open access: yesCase Rep Med
Objective: This case report describes a rare presentation of a cartilaginous choristoma of the oral cavity within the tonsillar fossa, emphasizing the importance of recognizing and differentiating this uncommon entity from more frequently encountered oral lesions. Methods: A comprehensive clinical and histopathological examination was conducted on a 30‐
Al-Ali M, Hantzakos A.
europepmc   +2 more sources

A case report of an oral hemangioma with unusual features. [PDF]

open access: yesClin Case Rep
Key Clinical Message A 26‐year‐old patient with swelling on the lingual surface of the mandible in the incisors area was referred to the Faculty of Dentistry at Mashhad University of Medical Sciences. After conducting clinical, radiographic, and pathological examinations, the patient was diagnosed with capillary hemangioma.
Salari S   +4 more
europepmc   +2 more sources

Successful treatment with MEK-inhibitor in a patient with NRAS-related cutaneous skeletal hypophosphatemia syndrome [PDF]

open access: yesGenes, Chromosomes and Cancer, Volume 61, Issue 12, Page 740-746, December 2022., 2022
Abstract Cutaneous skeletal hypophosphatemia syndrome (CSHS) is caused by somatic mosaic NRAS variants and characterized by melanocytic/sebaceous naevi, eye, and brain malformations, and FGF23‐mediated hypophosphatemic rickets. The MEK inhibitor Trametinib, acting on the RAS/MAPK pathway, is a candidate for CSHS therapy.
Brusco, Alfredo   +10 more
core   +2 more sources

Lingual Osseous Choristoma: Case report and literature review of this rare entity. [PDF]

open access: yesJ Clin Exp Dent, 2023
Intraoral osseous choristoma represents a benign lesion of growing ectopic bone in the soft tissues of the oral cavity. It is considered as rare entity while fewer than 100 cases have ever been reported worldwide.
Gkouveris I, Kapranos N, Mitrou GG.
europepmc   +3 more sources

Goldenhar Syndrome and Surgical Reconstruction: A Case Report of Bilateral Complete Eyelid Colobomas in a 2-Day-Old Patient. [PDF]

open access: yesCase Rep Ophthalmol Med
Goldenhar syndrome (GS), also known as Franceschetti–GS, encompasses a spectrum of congenital anomalies affecting the eyes, ears, face, and vertebrae. This case report highlights a 2‐day‐old female patient diagnosed with GS presenting a rare manifestation of bilateral complete eyelid colobomas.
Utt RS   +5 more
europepmc   +2 more sources

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