Cherubism: a rare case report with literature review

Lahfidi, Amal; Traore, Wend-Yam Mohamed; Diallo, Ibrahima Dokal; Lrhorfi, Najlae; Elhaddad, S; Allali, Nazik; Chat, Latifa

doi:10.1016/j.radcr.2022.07.063

Cited by 2 publications

(3 citation statements)

References 3 publications

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“…Cherubism-related syndromes include Ramon syndrome, Noonan syndrome, and neurofibromatosis type 1. Differential diagnosis includes myxoma, bilateral parotid swelling, giant cell recurrent granuloma, giant cell tumor, ameloblastoma, bilateral odontogenic cysts, histiocytosis X (Hand-Schuller-Christian disease), odontogenic keratocyst (including nevoid basal cell tumor syndrome), Jaffe-Campanacci syndrome, Brown tumor (hyperparathyroidism), infantile cortical hyperostosis, fibro-osteoma, ossified fibroma, fibrous dysplasia, odontogenic fibroma, and aneurysmal cysts [ 10 , 11 ]. While alkaline phosphatase levels are increased, biochemical tests can reveal normal ranges for blood follicle-stimulating hormone, phosphorus and calcium concentrations, luteinizing hormone, T4 and T3 levels, and thyroid-stimulating hormone.…”

Section: Discussionmentioning

confidence: 99%

Cherubism: Cone-Beam Computed Tomography Findings in Two Siblings

Mohod,

Dadgal

2024

Cureus

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Cherubism is an uncommon, multilocular cystic condition of the jaws. This autosomal dominant, nonneoplastic, fibro-osseous condition of the jaws affects children and is self-limiting. Clinically, it shows up as an expansion or distortion of the jaw together with an unnatural teeth alignment. In their most severe forms, these deformations might cause phonation difficulties, decreased pharynx lumen, visual issues, and psychological effects. This case report describes a case report of two siblings involving the maxilla and the mandible presenting with a painless bilateral symmetrical enlargement. Cherubism is a hereditary condition characterized by nonneoplastic bone lesions that damage the jaws. Surgery should be used to resolve any functional or aesthetically problematic issues. Typically, the surgical procedure is postponed until after puberty.

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Section: Discussionmentioning

confidence: 99%

Cherubism: Cone-Beam Computed Tomography Findings in Two Siblings

Mohod,

Dadgal

2024

Cureus

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“…In most cases, the progression of dysplasia tends to recede when the patient reaches puberty. Although lesions are usually asymptomatic and limited to the mandibular and maxillary bones, in severe cases, a misdiagnosis or late treatment may lead to the invasion of lesions to the orbital fossa, infrequently upper respiratory tract obstruction, and disruption of primary dentition along with inflammation and facial deformity leading to psychosocial and quality of life implications especially for young children [ 4 , 7 , 8 ].…”

Section: Discussionmentioning

confidence: 99%

“…The hallmark of the disease is symmetrical multilocular radiolucent lesions expanding in the mandible and maxilla [ 4 ]. This, besides the swelling of the submandibular lymph nodes in the early stages of the disease, contributes to the bizarre shape of the face [ 7 , 8 ].…”

Section: Introductionmentioning

confidence: 99%

Nonfamilial cherubism in a 6-month-old infant: a case report

Hamzavi,

Askari,

Bahrololoom

et al. 2024

BMC Pediatr

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Background Cherubism is known as a very rare autosomal dominant familial disorder of childhood caused by a mutation in the SH3BP2 gene on 4p16.3. It has not yet been observed at birth and is usually diagnosed in children aged 2–7. Here, we present a non-hereditary case of cherubism at a very early age. Case presentation A 6-month-old girl presented with bilateral progressive jaw enlargement. On physical examination, bilateral asymmetrical jaw enlargement, predominantly on the left side, and some enlarged, non-tender, mobile submandibular lymph nodes were detected. No other abnormality was observed. Further investigations with radiology suggested cherubism and Burkitt’s lymphoma as differential diagnoses. Later on, histopathologic evaluations were suggestive of cherubism. No surgical interventions were indicated, and the child is on regular follow-ups. Conclusion Non-hereditary Cherubism, despite scarcity, can present in children below two years of age, even as early as the beginning of primary dentition. Accurate and swift diagnosis is essential to avert physical and psychological complications. Our case report shows the importance of keeping cherubism in mind as a differential diagnosis of bone disease, even in children under a year old, and the value of interdisciplinary collaboration in dealing with rare genetic disorders.

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Cherubism: a rare case report with literature review

Cited by 2 publications

References 3 publications

Cherubism: Cone-Beam Computed Tomography Findings in Two Siblings

Cherubism: Cone-Beam Computed Tomography Findings in Two Siblings

Nonfamilial cherubism in a 6-month-old infant: a case report

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