Colagenomas: manifestación cutánea de neoplasia endocrina múltiple tipo 1 (MEN 1)

Authors

DOI:

https://doi.org/10.29176/2590843X.1539

Keywords:

Skin and connective tissue diseases, Skin neoplasms, Multiple endocrine neoplasia type 1

Abstract

Multiple endocrine neoplasia type 1 is a rare hereditary syndrome characterized by parathyroid, anterior pituitary and pancreatic tumors, that may also be associated with benign cutaneous neoplasms like angiofibromas and collagenomas, that can precede endocrine manifestations.

We present the case of a 23-year-old female patient with primary hyperparathyroidism, Cushing disease and a pancreatic neuroendocrine tumor associated with multiple collagenomas that appeared before systemic symptoms.

Author Biographies

Laura Pulgarín

Médico general, Universidad de Antioquia. Residente de Dermatología, Universidad del Valle.

Simón Gallo

Médico general. Residente de Dermatología, Centro de Investigaciones Dermatológicas CIDERM, Sección de Dermatología, Facultad de Medicina, Universidad de Antioquia.

Natalia Giraldo

Médico general. Residente de Dermatología, Centro de Investigaciones Dermatológicas CIDERM, Sección de Dermatología, Facultad de Medicina, Universidad de Antioquia.

Carlos Montealegre

Médico dermatólogo, Centro de Investigaciones Dermatológicas CIDERM, Sección de Dermatología, Facultad de Medicina, Universidad de Antioquia.

Alejandro Roman-González

Médico endocrinólogo, Universidad de Antioquia, Hospital Universitario San Vicente Fundación.

References

Marini F, Falchetti A, Del Monte F, Carbonell Sala S, Gozzini A, Luzi E, et al. Multiple endocrine neoplasia type 1. Orphanet J Rare Dis. 2006;1:38. doi: 10.1186/1750-1172-1-38

Darling TN, Skarulis MC, Steinberg SM, Marx SJ, Spiegel AM, Turner M. Multiple Facial Angiofibromas and Collagenomas in Patients With Multiple Endocrine Neoplasia Type 1. Arch Dermatol. 1997;133(7):853-7. doi:10.1001/archderm. 1997.03890430067009

Asgharian B, Turner ML, Gibril F, Entsuah L, Serrano J, Jensen R. Cutaneous Tumors in Patients with Multiple Endocrine Neoplasm Type 1 (MEN1) and Gastrinomas: Prospective Study of Frequency and Development of Criteria with High Sensitivity and Specificity for MEN1. J Clin Endocrinol Metab. 2004;89 (11):5328-36. doi: 10.1210/jc.2004-0218

Pack S, Turner ML, Zhuang Z, Vortmeyer AO, Boni R, Skarulis M, et al. Cutaneous tumors in patients with multiple endocrine neoplasia type 1 show allelic deletion of the MEN1 gene. J Invest Dermatol. 1998;110(4):438-40. doi: 10.1046/j.1523-1747.1998.00140.x

Nord B, Platz A, Smoczynski K, Kytölä S, Robertson G, Calender A, et al. Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma. Int J Cancer. 2000;87(4):463-7. doi: 10.1002/1097-0215(20000815)87:4<463::AIDIJC1>3.0.CO;2-8

Sakurai A, Matsumoto K, Ikeo Y, Nishio SI, Kakizawa T, Arakura F, et al. Frequency of facial angiofibromas in Japanese patients with multiple endocrine neoplasia type 1. Endocr J. 2000;47(5):569-73. doi: 10.1507/endocrj.47.569

Vidal A, Iglesias MJ, Fernández B, Fonseca E, Cordido F. Cutaneous lesions associated to multiple endocrine neoplasia syndrome type 1. J Eur Acad Dermatol Venereol. 2008;22(7):835-8. doi: 10.1111/j.1468-3083.2008.02578.x

Roman JW, Logemann NF, Adams E. Incidental angiofibromas prompt a diagnosis of multiple endocrine neoplasia type-1 (MEN-1). Dermatol Online J. 2014;20(9):13030/qt4kq2z97b

How to Cite

1.
Pulgarín L, Gallo S, Giraldo N, Montealegre C, Roman-González A. Colagenomas: manifestación cutánea de neoplasia endocrina múltiple tipo 1 (MEN 1). rev. asoc. colomb. dermatol. cir. dematol. [Internet]. 2020 Dec. 10 [cited 2024 Jul. 22];28(3):269-73. Available from: https://revista.asocolderma.org.co/index.php/asocolderma/article/view/1539

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Published

2020-12-10

How to Cite

1.
Pulgarín L, Gallo S, Giraldo N, Montealegre C, Roman-González A. Colagenomas: manifestación cutánea de neoplasia endocrina múltiple tipo 1 (MEN 1). rev. asoc. colomb. dermatol. cir. dematol. [Internet]. 2020 Dec. 10 [cited 2024 Jul. 22];28(3):269-73. Available from: https://revista.asocolderma.org.co/index.php/asocolderma/article/view/1539
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