Generalized Lymphadenopathy in Infancy; a Case Report

Author(s):
Setareh MamishiSetareh Mamishi1, Zahra MovahediZahra Movahedi2, Vahid MohammadzadehVahid Mohammadzadeh3, Farah SabouniFarah Sabouni4,*
*Corresponding Author: Email: [email protected]

Innovative Journal of Pediatrics:Vol. 23, issue 1; 105-108
Published online:Dec 15, 2012
Article type:Case Report
Received:Aug 24, 2011
Accepted:Jul 17, 2012
How to Cite:Mamishi S, Movahedi Z, Mohammadzadeh V, Sabouni F. Generalized Lymphadenopathy in Infancy; a Case Report. Inn J Pediatr. 2013;23(1):. doi:

Abstract

Background: Rosai-Dorfman disease (RDD) is a rare disease of histiocytic cells, a cause of benign cervical lymphadenopathy (LAP) and massive generalized lymph node enlargement in children and adults. There are also some reports on involvement of other human body organs with or without LAP.
Case Presentation: A 7-month-old infant with chief complaint of generalized massive LAP was referred to our center. RDD was diagnosed according to clinical manifestations and confirmed through histopathologic and immunoreactivity study on the obtained sample by cervical lymph node biopsy.
Conclusion: RDD is not a malignant illness and lymph node enlargement most often decreases in its size happens without special treatment.

 

References

  • 1.
    References are available on the PDF.

Copyright

© 2013, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

Similar Articles

30
Dec
2005

A Rare Presentation of Rosai- Dorfman Syndrome: First Reported Case in Iran

Alireza Zahiri,
H Rahmat,
A Shojaiee

Zahiri A, Rahmat H, Shojaiee A. A Rare Presentation of Rosai- Dorfman Syndrome: First Reported Case in Iran. I J Radiol. 2005;3(1):e79073. doi:

12
Jun
2024
J Skin Stem

An Update on the Etiopathogenesis and Management of Morbihan Disease: A Narrative Review

Mohammed Abu El-Hamd,
Soha Aboeldahab

Abu El-Hamd M, Aboeldahab S. An Update on the Etiopathogenesis and Management of Morbihan Disease: A Narrative Review. J Skin Stem Cell. 2024;11(2):e146014. doi: https://doi.org/10.5812/jssc-146014

3
Jan
2013

Cutaneous Sarcoid-Like Granulomas in a Child Known with Nijmegen Breakage Syndrome

Andreea Liana Rachisan,
Dan Gheban,
Nicolae Miu

Liana Rachisan A, Gheban D, Miu N. Cutaneous Sarcoid-Like Granulomas in a Child Known with Nijmegen Breakage Syndrome. Inn J Pediatr. 2013;23(1):. doi:

5
Jun
2004

A case of Burkitt’s lymphoma

h Heyrani moqadam,
Behzad Narouie

Heyrani moqadam H, Narouie B. A case of Burkitt’s lymphoma. Zahedan J Res Med Sci. 2004;6(2):e95015. doi:

25
Jul
2015

A Case of Recurrent Kikuchi-Fujimoto Disease

Majid Reza Erfanian Taghvaei,
Maryam Mirzaie,
Ali Parsa,
Taghi Ghiasi Moghadam

Erfanian Taghvaei MR, Mirzaie M, Parsa A, Ghiasi Moghadam T. A Case of Recurrent Kikuchi-Fujimoto Disease. Jundishapur J Microbiol. 2015;8(7):e25654. doi: https://doi.org/10.5812/jjm.25654v2

Download PDF220.45 KB
Share on
Cited by
Metrics

Ordering Reprints

Articles are published under the Creative Commons license stated on each article. No permission or royalty fee is required for uses permitted by that license. CCC handles optional bulk and customized reprint orders. Any quotation covers production and delivery services only, not copyright permission. > Request Reprints from CCC 

Search Relations

Author(s):

Related Articles