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Case Reports
. 2019 Jan;98(3):e13997.
doi: 10.1097/MD.0000000000013997.

Slipped capital femoral epiphysis in an adult with congenital hypopituitarism: A case report

Affiliations
Case Reports

Slipped capital femoral epiphysis in an adult with congenital hypopituitarism: A case report

Yi-Fan Huang et al. Medicine (Baltimore). 2019 Jan.

Abstract

Rationale: Slipped capital femoral epiphysis (SCFE) is a common hip problem in adolescents, usually individuals between 8 and 15 years old. Because of the frequent finding of growth abnormalities in affected children, various endocrine disturbances have been reported as the cause of the disease. However, there are few case reports of older patients in previous literature. To the best of our knowledge, congenital hypopituitarism with normal growth hormone (GH) level has not been reported.

Patient concerns: We describe a 29-year-old man who had a 3-month history of pain in the left hip with tall stature and unobvious secondary sexual characteristics. Laboratory testing showed low thyroxine, low cortisol, low follicle-stimulating hormone, low luteinizing hormone, low testosterone, but normal GH.

Diagnoses: Brain magnetic resonance imaging showed pituitary hypoplasia. An anteroposterior pelvis radiograph showed severe varus SCFE in the left hip, it was also confirmed with computed tomography scans.

Interventions: The patient was treated with levothyroxine, hydrocortisone, and testosterone replacement therapy before surgery. We performed open reduction and anatomical reduction by Dunn's procedure.

Outcome: We have followed this patient for 6 months, the left hip mobility gradually improved. No slip in the contralateral proximal femoral physis has been observed.

Lessons: When unobvious secondary sexual characteristics and body abnormalities were found in clinical practice, endocrine condition should be evaluated, since the contralateral side may prone to slip due to the lack of endocrine therapy.

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Conflict of interest statement

The authors have no funding and conflicts of interest to disclose.

Figures

Figure 1
Figure 1
An anteroposterior radiograph of the pelvis showed left, severe, varus slipped capital femoral epiphysis.
Figure 2
Figure 2
Transverse computed tomography scans confirm left proximal femoral physeal union.
Figure 3
Figure 3
Anteroposterior radiograph of the left wrist prompted that his bone age was 13 years and 6 months.
Figure 4
Figure 4
Brain magnetic resonance imaging showed pituitary hypoplasia.
Figure 5
Figure 5
The postoperative anteroposterior radiograph of the pelvis showed good rehabilitation.

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References

    1. Loder RT, Skopelja EN. The epidemiology and demographics of slipped capital femoral epiphysis. ISRN Orthop 2011;2011:486512. - PMC - PubMed
    1. Witbreuk M, van Kemenade FJ, van der Sluijs JA, et al. Slipped capital femoral epiphysis and its association with endocrine, metabolic and chronic diseases: a systematic review of the literature. J Child Orthop 2013;7:213–23. - PMC - PubMed
    1. Marquez D, Harb E, Vilchis H. Slipped capital femoral epiphysis and hypothyroidism in a young adult: a case report. J Med Case Rep 2014;8:336. - PMC - PubMed
    1. Soleymanha M, Karimi A, Mehrdad SM. A case of slipped capital femoral epiphysis in association with craniopharyngioma. Trauma Monthly 2015;20:e25633. - PMC - PubMed
    1. Song MH, Jang WY, Park MS, et al. Slipped capital femoral epiphysis in children younger than 10 years old: clinical characteristics and efficacy of physeal-sparing procedures. J Pediatr Orthop B 2018;27:379–86. - PubMed

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