Case Report
Volume 12 Issue 11 - 2021
Unicentric Castleman’s Disease with Multicentric Behavior: A Case Report
Raed M Alzyoud1*, Hamza M Al-Nsour1, Rawand M AlQtaishat1, Lina I Ghanmiyin1, Zeyad M Khalilah2, Motasem O Alsuweiti1, Mohammed D Al Nahar3 and Omar Ashokaibi4
1Pediatric Immunology, Allergy, and Rheumatology Division, Queen Rania Children’s Hospital, Amman, Jordan
2Pediatric Pulmonary Division, Queen Rania Children’s Hospital, Amman, Jordan
3Externship Physician, Queen Rania Children’s Hospital, Amman, Jordan
4Pathology Division, Princess Iman Research and Laboratory Science Center, Amman, Jordan
*Corresponding Author: Raed M Alzyoud, Pediatric Immunology, Allergy and Rheumatology section, Queen Rania Children’s Hospital, Amman, Jordan.
Received: September 09, 2021; Published: October 29, 2021




Abstract

Castleman’s disease is a clinicopathological entity associated with lymphoproliferation. We report a case of a 13-year-old who was initially clinically suspected to have Behçet Disease (BD) (owing to clinical features at presentation), though was later histologically confirmed to have Castleman’s disease. This case report shows how unicentric Castleman’s disease can share behaviors similar to the multicentric disease.

Keywords: Unicentric Castleman Disease; Behçet Disease; Paraneoplastic Syndrome

References

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  11. Nikolskaia OV., et al. “Paraneoplastic pemphigus in association with Castleman’s disease”. British Journal of Dermatology 149 (2003): 1143‑11
  12. Hiroki Mochizuki., et al. “Overlap of IgG4-related Disease and Multicentric Castleman’s Disease in a Patient with Skin Lesions”. Internal Medicine 9 (2017): 1095-1099.
  13. Zumi Y., et al. “Multicentric Castleman disease mimicking IgG4-related disease: A case report”. Modern Rheumatology 21 (2017): 174-177.
Citation: Raed M Alzyoud., et al. “Unicentric Castleman’s Disease with Multicentric Behavior: A Case Report”. EC Orthopaedics 12.11 (2021): 57-62.

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