Tuberous sclerosis with oral manifestations: A rare case report

Sodhi, Sps; Dang, Ramandeep Singh; Brar, Gursimrat Kaur

doi:10.4103/2229-516x.174018

Cited by 3 publications

(2 citation statements)

References 9 publications

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“…[56] It is more common in females and usually diagnosed between 4 and 10 years of age or in puberty. [2] TSC can be diagnosed on the basis of clinical features (major and minor characteristics) and some investigations.…”

Section: Discussionmentioning

confidence: 99%

Odontogenic myxofibroma of gingiva in a pediatric patient with tuberous sclerosis: A rare case report

2016

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Tuberous sclerosis complex (TSC) is a rare multisystem genetic disease, with an estimated incidence of 1 in 6000–1 in 10,000. TSC is an autosomal dominant syndrome involving heart, kidneys, lungs, and skin. The classic triad of TSC is seizures, mental retardation, and angiofibromas; this triad occurs in only 29% of patients. The clinical diagnostic guidelines on TSC are prepared based on clinical features, radiographic findings. The most common oral manifestations of TSC are fibroma, gingival hyperplasia, and enamel hypoplasia. Odontogenic myxofibroma represents a rare slow-growing benign neoplasm found rarely in children below 10 years or adults over 50 years of age. The prevalence of myxoma is between 0.04% and 3.7%. Here, we are reporting a rare case of myxofibroma of gingiva in an 8-year-old female TSC patient.

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Section: Discussionmentioning

confidence: 99%

Odontogenic myxofibroma of gingiva in a pediatric patient with tuberous sclerosis: A rare case report

2016

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“…Oral manifestations of TS occur in 11% of affected subjects, and oral abnormalities include the presence of delayed eruption, bifid uvula, enamel hypoplasia, cystic hyperostosis, hyperplasia, enamel pitting, haemangioma, multiple osteomas, cleft lip and palate, and desmoplastic fibromas (DF) [ 2 , 4 ]. The combination of desmoplastic fibroma and tuberous sclerosis is uncommon; there is little information about its clinical features.…”

Section: Introductionmentioning

confidence: 99%

Desmoplastic Fibroma Recurrence Associated with Tuberous Sclerosis in a Young Patient

Espinoza-Coronado

Loyola-Rodríguez

Olvera-Delgado

et al. 2018

Case Reports in Dentistry

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Case Report. A nine-year-old patient with a diagnosis of tuberous sclerosis (with no pathological record) that showed calcifications at the brain level. Besides, the case showed the Vogt triad (epilepsy, mental retardation, and sebaceous adenoma). The patient clinically showed a volume increase of hard consistency, without suppuration and no sessile that included the following teeth 73, 74, and 75. Cone beam computed tomography (CBCT) was obtained, and it displayed a delimited unilocular lesion. After surgical excision, the histopathological report was desmoplastic fibroma (DF). It was observed that the patient had an aggressive recurrence of DF at four months after surgery treatment. Due to these clinical findings, resective osseous surgery and curettage were carried out. It is uncommon to find these two pathologies together (DF and tuberous sclerosis). Since DF is a benign pathology but very invasive and destructive, it is necessary a constant follow-up examination due to a high recurrence frequency.

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Clinical pathologic conference: diffuse papillomatous lesions of the gingiva with posterolateral neck skin tags

Lin

Mort

Hinchey

et al. 2018

Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology

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Tuberous sclerosis with oral manifestations: A rare case report

Cited by 3 publications

References 9 publications

Odontogenic myxofibroma of gingiva in a pediatric patient with tuberous sclerosis: A rare case report

Odontogenic myxofibroma of gingiva in a pediatric patient with tuberous sclerosis: A rare case report

Desmoplastic Fibroma Recurrence Associated with Tuberous Sclerosis in a Young Patient

Clinical pathologic conference: diffuse papillomatous lesions of the gingiva with posterolateral neck skin tags

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