Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Odontogenic Cysts in Gorlin Goltz Syndrome - Clinicoradiological Presentation and Management

View through CrossRef
Gorlin–Goltz syndrome, or nevoid basal cell carcinoma syndrome, is an uncommon autosomal dominant disorder characterized by multiple odontogenic keratocysts, basal cell carcinomas, and a spectrum of skeletal and developmental anomalies. We present the case of a 13-year-old male who reported with progressive mandibular swellings and facial asymmetry. Clinical examination and panoramic radiography revealed multiple well-circumscribed radiolucent lesions involving both jaws, consistent with odontogenic keratocysts. The diagnosis was established based on clinic-radiological findings and confirmed histo-pathologically. Surgical enucleation of the cysts was performed with adjunctive measures to reduce the risk of recurrence. This case underscores the importance of early recognition of Gorlin–Goltz syndrome in paediatric patients, the necessity of multidisciplinary management, and the imperative for long term surveillance to mitigate morbidity and detect associated systemic manifestations.
Title: Odontogenic Cysts in Gorlin Goltz Syndrome - Clinicoradiological Presentation and Management
Description:
Gorlin–Goltz syndrome, or nevoid basal cell carcinoma syndrome, is an uncommon autosomal dominant disorder characterized by multiple odontogenic keratocysts, basal cell carcinomas, and a spectrum of skeletal and developmental anomalies.
We present the case of a 13-year-old male who reported with progressive mandibular swellings and facial asymmetry.
Clinical examination and panoramic radiography revealed multiple well-circumscribed radiolucent lesions involving both jaws, consistent with odontogenic keratocysts.
The diagnosis was established based on clinic-radiological findings and confirmed histo-pathologically.
Surgical enucleation of the cysts was performed with adjunctive measures to reduce the risk of recurrence.
This case underscores the importance of early recognition of Gorlin–Goltz syndrome in paediatric patients, the necessity of multidisciplinary management, and the imperative for long term surveillance to mitigate morbidity and detect associated systemic manifestations.

Related Results

Cometary Physics Laboratory: spectrophotometric experiments
Cometary Physics Laboratory: spectrophotometric experiments
<p><strong><span dir="ltr" role="presentation">1. Introduction</span></strong&...
Gorlin Goltz Syndrome: A Disease in Disguise
Gorlin Goltz Syndrome: A Disease in Disguise
Gorlin Goltz syndrome also known as nevoid basal cell carcinoma is an autosomal dominant inherited disorder caused due to mutation in patched (PTCH) tumor suppressor gene present i...
Glandular Odontogenic Cyst
Glandular Odontogenic Cyst
A cyst is a Pathological cavity which consists of solid, semi-solid or gaseous contents which are not createdby the accumulation of pus and which may or may not be lined by epithel...
Histopathologic and immunohistochemical findings of odontogenic jaw cysts treated by decompression technique
Histopathologic and immunohistochemical findings of odontogenic jaw cysts treated by decompression technique
Context: Odontogenic cysts are among the most common lesions to affect the oral and maxillofacial region. Cysts are capable of causing significant bony disfigurement, t...
Gorlin–Goltz Syndrome with Eyelid Coloboma and Café au Lait Macule: Case Report and Literature Review
Gorlin–Goltz Syndrome with Eyelid Coloboma and Café au Lait Macule: Case Report and Literature Review
Gorlin–Goltz syndrome (GGS), also known as Nevoid basal cell carcinoma syndrome (NBCCS), or Gorlin syndrome, is a rare autosomal dominant inherited genodermatosis characterized by ...
A Rare Case of Focal Dermal Hypoplasia: Goltz Syndrome; Goltz Gorlin Syndrome
A Rare Case of Focal Dermal Hypoplasia: Goltz Syndrome; Goltz Gorlin Syndrome
: Focal dermal hypoplasia, popularly known as the goltz syndrome, is an extremely rare multisystem disorder mainly involving the skin, skeletal system, and eyes. Being an X-linked ...
Hydatid Disease of The Brain Parenchyma: A Systematic Review
Hydatid Disease of The Brain Parenchyma: A Systematic Review
Abstarct Introduction Isolated brain hydatid disease (BHD) is an extremely rare form of echinococcosis. A prompt and timely diagnosis is a crucial step in disease management. This ...
Cytology of lepidoptera. III. Giant cysts: A morphological trait of apyrene spermatogenesis in an Ephestia kuehniella strain
Cytology of lepidoptera. III. Giant cysts: A morphological trait of apyrene spermatogenesis in an Ephestia kuehniella strain
AbstractA comparative investigation of testicular eupyrene cysts (in larvae) and apyrene cysts (in pupae) of Ephestia kuehniella laboratory strains was conducted using light and el...

Back to Top