Abstract
Abstract
Background
Histiocytic system consists of phagocytes and dendritic cells. Both are found in lymph nodes. Usually, this disorder presents with painless cervical lymph node enlargement hence frequently mistaken for lymphoma or tuberculosis.
Case presentation
Here, we report three pediatric cases: one of Langerhans cell histiocytosis and two of sinus histiocytosis and massive lymphadenopathy with neck mass as initial presentation. The final diagnosis was made with fine needle aspiration cytology, biopsy, and ancillary tests.
Conclusion
Biopsy and immunohistochemistry studies are recommended for determining subtypes of histiocytosis and further management of patient.
Publisher
Springer Science and Business Media LLC
Reference9 articles.
1. Jackson MA, Long S, Prober C, Fischer M. Principles and practice of pediatric infectious diseases, 5th edn. Chapter 12. 2018. p. 102
2. Histiocytic disorders, Histiocytosis Association Incorporated; info@histio.org, https://www.histio.org/page.aspx?pid=378#.XzJcEygzY2w
3. Emile JF, Abla O, Fraitag S, Horne A (2016) Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages. Histiocyte Society; Blood. 127(22):2672–81
4. Kumar YP, Agrawal J, Mohanlakshmi J, Kumar PS (2015) Langerhans cell histiocytosis revisited: case report with review. Contemp Clin Dent. 6(3):432–436. https://doi.org/10.4103/0976-237X.161912
5. Lima, Felipe Barbosa et al. “Rosai-Dorfman disease with spontaneous resolution: case report of a child.” Revista brasileira de hematologia e hemoterapia vol. 33,4 (2011): 312-4. https://doi.org/10.5581/1516-8484.20110083