Results 41 to 50 of about 5,727 (190)
Mixed heterotopic gastrointestinal cyst and extranasal glial tissue of oral cavity with cleft palate
Mixed choristomas of the oral cavity are uncommon lesions that show a variety of clinical presentations, histological appearance and growth patterns. Mixed choristoma with cleft palate is a very rare developmental malformation.
Teerthanath Srinivas +2 more
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A Case of Osseous Choristoma of Submental Region- Cone Beam Computed Tomographic Findings [PDF]
Soft tissue radiopacities of head and neck region are intriguing to the oral and maxillofacial radiologist. Osseous choristoma is seldom included in the list of probable differential diagnosis, since its occurrence in the region is a rare phenomenon ...
Gunjan Sinha +2 more
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Bukkal Mukozada Osseous Choristoma vakası
SüleymanDemirel Üniversitesi TIP FAKÜLTESİ DERGİSİ: 2005 Eylül; 12(3) Bukkal Mukozada Osseous Choristoma vakası Ozden Candır, Nermin Karahan, Harun Doğru, Serife Aydin ÖzetChoristoma anormal lokalizasyonda gelişen normal hücre kitlesi gibi ...
Karahan, Nermin +3 more
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ABSTRACT Distinguishing benign intranodal thyroid inclusions from metastatic papillary thyroid carcinoma is vital in synchronous malignancies to prevent overstaging. Integrating morphological analysis with BRAF VE1 immunohistochemistry ensures diagnostic precision to align management with the true pathological stage, avoiding unnecessary aggressive ...
Bo‐Cheng Rau +2 more
wiley +1 more source
Congenital neuroglial choristoma of the foot
Neuroglial choristomas are rare malformations of heterotopic neural tissue that have been previously reported predominantly in the head and neck. Competing theories of embryogenesis propose their origin as encephaloceles that have undergone resorption of
Justin Glavis-Bloom, MD +4 more
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Salivary Gland Choristoma: A Rare Finding at the Gastroesophageal Junction.
A choristoma is a tumor-like outgrowth consisting of heterotopic, histologically mature tissue located at an anatomically unusual part of the body. Salivary gland choristoma at the gastrointestinal junction (GEJ) is an extremely rare entity with only one
Hanke, Rachel +4 more
core +1 more source
ABSTRACT A congenital inferolateral‐neck papule with a visible or palpable firm subcutaneous cord should prompt consideration of a cartilaginous remnant. This cord‐like extension may mimic a branchial sinus tract, but clinicopathological correlation is required to distinguish cervical chondrocutaneous branchial remnant from an epithelial‐lined sinus ...
Ruoyu Wan +4 more
wiley +1 more source
Epibulbar complex choristoma with simultaneous involvement of eyelid: a case report
Background Epibulbar complex choristoma, a rare congenital epibulbar tumor, has many diverse forms. Reviewing the literature, it can present clinically as either a circumferential or isolated epibulbar mass, limbal tumor, lateral canthal mass, aggregate ...
Yun Hsia +4 more
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Epidermoid cyst as differential diagnosis for spherical keratoma: What do we know?
Summary This article briefly presents the case of a space‐occupying coronary band mass that raised the question of how one can differentiate between two uncommonly seen but now commonly paired differential diagnoses and prompted a review of the relevant literature.
R. Goodman‐Davis +2 more
wiley +1 more source
A Unique Case of Conjuctival Choristoma Masquerading As Nasal Pterygium
Being at the distinctive position of covering the eye ball, conjunctiva is frequently involved in array of local and systemic disorders. Tumors of cornea and conjunctiva often present the ophthalmologist with a difficult diagnostic and therapeutic ...
Mukta Sharma, Shruti Anand
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