Coexistence of Slipped Capital Femoral Epiphysis and multiple endocrine neoplasia type 2B (MEN2B) - a case report
نویسندگان
چکیده
Introduction: MEN 2B syndrome is distinguished by the occurrence of medullary thyroid cancer, pheochromocytoma, mucosal neuromas, marfanoid features, and skeletal anomalies, including kyphoscoliosis, joint laxity, pes cavus, and, in a smaller number cases, slipped capital femoral epiphysis (SCFE).
 Case report: We describe case report 15-years-old patient with diagnosis MEN2B rare manifestation Slipped Capital Femoral Epiphysis (SCFE). A 15-year-old female presented to orthopedics out-patient department (OPD) complaints pain around right hip knee walking limp for approximately four months. Additionally, feeling enlarged gland was reported. X-ray confirmed presence SCFE, while biopsy revealed cancer (MTC). Thus, made.
 Conclusion: (SCFE) can occasionally be syndrome. It important physicians aware this association, as it contribute early detection potentially life-threatening condition.
منابع مشابه
Slipped Capital Femoral Epiphysis and Primary Hyperparathyroidism: A Case Report
The aim of reporting this case is to highlight the association of two disorders, primary hyperparathyroidism (PHPT) and slipped capital femoral epiphysis (SCFE). They are usually seen in two different age groups and rarely together. PHPT is a rare cause of SCFE and only 10 cases have been reported in the literature worldwide. The patient in our report is a 13-year-old girl who presented to our ...
متن کامل[Slipped capital femoral epiphysis].
Slipped capital femoral epiphysis (SFCE) is a disorder of the hip, characterized by a displacement of the capital femoral epiphysis from the metaphysic through the femoral growth plate. The epiphysis slips posteriorly and inferiorly. SCFE occurs during puberty and metabolic and epidemiologic risk factors, such as obesity are frequently found. Most chronic slips are diagnosed late. Sagittal hip ...
متن کاملSlipped capital femoral epiphysis.
SCFE is the most common hip abnormality in adolescence. The subsequent development and severity of degenerative changes is related to the degree of slippage and to delay in diagnosis. Awareness of this diagnostic possibility in the population at greatest risk and knowledge of subtle and early radiographic findings will allow prompt diagnosis and treatment of SCFE. Follow-up radiographic examina...
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We present a 15-year-old female patient with medullary thyroid carcinoma, marfanoid habitus, and mucosal ganglioneuromatosis. Our case had a RET protooncogene mutation ser836 polymorphism in exon 14 and ser904 polymorphism in exon 15. Our patient is thought to be atypical MEN2B due to the absence of M918T or A883F mutations. Chilaiditi sign is an incidental radiographic finding of a usually asy...
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ژورنال
عنوان ژورنال: Journal of Education, Health and Sport
سال: 2023
ISSN: ['2391-8306']
DOI: https://doi.org/10.12775/jehs.2023.39.01.012