Primary pigmented nodular adrenocortical disease associated with Carney complex

case report and literature review

Authors

  • Fabrícia Torres Gonçalves Hospital de Clínicas, Universidade Federal de Uberlândia
  • Taciana Carla Maia Feibelmann Hospital de Clínicas, Universidade Federal de Uberlândia
  • Cínthia Monteiro Mendes Hospital de Clínicas, Universidade Federal de Uberlândia
  • Maria Luiza Mendonça Pereira Fernandes Hospital de Clínicas, Universidade Federal de Uberlândia
  • Geraldo Henrique Gouvêa de Miranda Hospital de Clínicas, Universidade Federal de Uberlândia
  • Agostinho Pinto Gouvêa Hospital de Clínicas, Universidade Federal de Uberlândia
  • Paulo Tannús Jorge Hospital de Clínicas, Universidade Federal de Uberlândia

Keywords:

Cushing’s syndrome, Hyperplasia, Adrenalectomy, Adrenal cortex diseases, Lentigo

Abstract

CONTEXT: Carney complex (CNC), a familial multiple neoplasm syndrome with dominant au- tosomal transmission, is characterized by tumors of the heart, skin, endocrine and peripheral nervous system, and also cutaneous lentiginosis. This is a rare syndrome and its main endocrine manifestation, primary pigmented nodular ad- renal disease (PPNAD), is an uncommon cause of adrenocorticotropic hormone-independent Cushing’s syndrome. CASE REPORT: We report the case of a 20 year old patient with a history of weight gain, hirsutism, acne, secondary amenorrhea and facial lentiginosis. Following the diagnosing of CNC and PPNAD, the patient underwent laparoscopic bilateral adrenalectomy, and she evolved with decreasing hypercortisolism. Screening was also performed for other tumors related to this syndrome. The diagnostic criteria, screening and follow-up for patients and af- fected family members are discussed.

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Author Biographies

Fabrícia Torres Gonçalves, Hospital de Clínicas, Universidade Federal de Uberlândia

MD. Attending physician, postgraduate endocrinology student, Department of Endocrinology, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.

Taciana Carla Maia Feibelmann, Hospital de Clínicas, Universidade Federal de Uberlândia

MD. Attending physician postgraduate endocrinology student, Department of Endocrinology, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.

Cínthia Monteiro Mendes, Hospital de Clínicas, Universidade Federal de Uberlândia

Undergraduate student, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.

Maria Luiza Mendonça Pereira Fernandes, Hospital de Clínicas, Universidade Federal de Uberlândia

MD, MSc. Attending Physician, Department of Endocrinology, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.

Geraldo Henrique Gouvêa de Miranda, Hospital de Clínicas, Universidade Federal de Uberlândia

MD. Attending Physician (Surgeon), Department of Surgery, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

Agostinho Pinto Gouvêa, Hospital de Clínicas, Universidade Federal de Uberlândia

MD, PhD. Professor of Pathology, Department of Pathology, Hospital das Clínicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

Paulo Tannús Jorge, Hospital de Clínicas, Universidade Federal de Uberlândia

MD, PhD. Professor of Postgraduate Programs in Medical Science, Department of Endocrinology, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brazil.

References

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Stratakis CA, Courcoutsakis NA, Abati A, et al. Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex). J Clin Endocrinol Metab. 1997;82(7):2037-43.

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Published

2006-11-11

How to Cite

1.
Gonçalves FT, Feibelmann TCM, Mendes CM, Fernandes MLMP, Miranda GHG de, Gouvêa AP, Jorge PT. Primary pigmented nodular adrenocortical disease associated with Carney complex: case report and literature review. Sao Paulo Med J [Internet]. 2006 Nov. 11 [cited 2025 Oct. 15];124(6):336-9. Available from: https://periodicosapm.emnuvens.com.br/spmj/article/view/2287

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Case Report