Innovative Journal of Pediatrics
The Scientific Journal of Growth & Development Research Center
e-ISSN 3117-5341
Image Credit:Inn J Pediatr
Outline
Generalized Lymphadenopathy in Infancy; a Case Report
Authors
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.
Highlights
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
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
Cited by
- Scopus by DOI: 0
Last Update: 1 week ago
- Scopus by Title: 3
Last Update: 1 week ago
- Scopus by Title (Ref): 0
Last Update: 1 week ago
- CrossRef: 0
Last Update: 8 hours ago
- OpenAlex: 0
Last Update: 11 hours ago
- OpenCitations: 0
Last Update: 5 days ago
Comments
Number of Comments:0