Make your own diagnosis: part I

Authors

DOI:

https://doi.org/10.29176/2590843X.1837

Keywords:

emperipolesis, Histiocitosis sinusal con linfadenopatía masiva, Enfermedad cutánea de Rosai-Dorfman

Abstract

It is a rare and generally benign histiocytic proliferative disorder that mainly affects the cervical lymph nodes, however, it can have skin involvement in 10% of cases, it is associated with nonspecific systemic symptoms and symptoms in some paraclinical symptoms. A cutaneous form without symptoms or systemic commitment has been described, which is shown in this case. Its etiology is unknown, although several theories have been proposed. It typically involves the face and trunk, manifests as asymptomatic reddish-brown to yellow papules, plaques, or nodules. This entity has a chronic course, there is no specific treatment, it must be individualized according to the severity and extension of the lesions and in many cases clinical surveillance is proposed.

Author Biographies

Erika Muñoz-Herrera, Universidad de Antioquia, Medellín, Colombia.

Residente de Dermatología, Universidad de Antioquia, Medellín, Colombia.

Emil Jiménez-Berástegui, Universidad de Antioquia, Medellín, Colombia.

Residente de Patología, Universidad de Antioquia, Medellín, Colombia.

Juan David Ruiz-Restrepo, Universidad de Antioquia, Medellín, Colombia.

Patólogo, Fundación Colombiana de Cancerología Clínica Vida. Docente, Dermatopatología, Universidad de Antioquia, Medellín, Colombia.

References

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Kong YY, Kong JC, Shi DR, Lu HF, Zhu XZ, Wang J, Chen ZW. Cutaneous rosai-dorfman disease: a clinical and histopathologic study of 25 cases in China. Am J Surg Pathol. 2007 Mar;31(3):341-50. doi: 10.1097/01.pas.0000213387.70783.b6. PMID: 17325475.

Yasodha Natkunam, et al. Rosai-Dorfman Disease. In: WHO Classification of Tumours Editorial Board. Skin tumours [Internet; beta version ahead of print]. Lyon (France): International Agency for Research on Cancer; 2023 [cited 2023/03/21]. (WHO classification of tumours series, 5th ed.; vol. 12). Available from: https://tumourclassification.iarc.who.int/chapters/64.

Leal PA, Adriano AL, Breckenfeld MP, Costa IS, de Sousa AR, Gonçalves Hde S. Rosai-Dorfman disease presenting with extensive cutaneous manifestation - case report. An Bras Dermatol. 2013;88(2):256-259. doi:10.1590/S0365-05962013000200014.

Fening K, Bechtel M, Peters S, Zirwas M, Darabi K. Cutaneous rosai-dorfman disease persisting after surgical excision: report of a case treated with acitretin. J Clin Aesthet Dermatol. 2010 Sep;3(9):34-6. PMID: 20877523; PMCID: PMC2945846.

How to Cite

1.
Muñoz-Herrera E, Jiménez-Berástegui E, Ruiz-Restrepo JD. Make your own diagnosis: part I. rev. asoc. colomb. dermatol. cir. dematol. [Internet]. 2024 Jun. 27 [cited 2024 Jul. 2];32(2):121-2. Available from: https://revista.asocolderma.org.co/index.php/asocolderma/article/view/1837

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Published

2024-06-27

How to Cite

1.
Muñoz-Herrera E, Jiménez-Berástegui E, Ruiz-Restrepo JD. Make your own diagnosis: part I. rev. asoc. colomb. dermatol. cir. dematol. [Internet]. 2024 Jun. 27 [cited 2024 Jul. 2];32(2):121-2. Available from: https://revista.asocolderma.org.co/index.php/asocolderma/article/view/1837

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Make the diagnosis yourself. Part 1
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