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Revista Cubana de Investigaciones Biomédicas

ISSN 1561-3011 (Electronic)
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2020, Number 2

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Rev Cubana Invest Bioméd 2020; 39 (2)

Presentation of a case of Cooke-Apert-Gallais syndrome

Ramos RA, del Busto MA
Full text How to cite this article

Language: Spanish
References: 3
Page: 1-6
PDF size: 183.06 Kb.


Key words:

hyperandrogenism, hirsutism, endocrinopathy.

ABSTRACT

A study was conducted of a female 47-year-old patient with a history of good health and no personal or family atopic antecedents, who attends endocrinology consultation due to increased growth of body hair of two years' evolution. Physical examination revealed facial reddishness, a male pubic shield, predominance of the scapular waist over the abdominal waist, and 3.5 cm hypertrophy of the clitoris. Complementary tests found a marked increase in blood testosterone, which led to the performance of hysterectomy with double adnexectomy. The result of the biopsy was benign Leydig cell tumor. The final diagnosis was Cooke-Apert-Gallais syndrome due to a testosterone-producing tumor in the ovary.


REFERENCES

  1. Llanio Navarro R, Perdomo Gonzáles G, Propedéutica clínica y semiología médica (Tomo 1).La Habana, Cuba: Editorial Ecimed; 2003.

  2. Endocrinología y metabolismo. Manual CTO de Medicina y Cirugía. Colectivo de autores. España: Madrid; 2014; Editorial CTO.

  3. Escobar-Morreale HF, Carmina E, Dewailly D, Gambineri A, Kelestimur F, Moghetti P, et al. Epidemiology, diagnosis and management of hirsutism: a consensus statement by the Androgen Excess and Polycystic Ovary Syndrome Society. Hum Reprod Update. 2012; 18(2):146-70.




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Rev Cubana Invest Bioméd. 2020;39