Click for new scientific resources and news about Corona[COVID-19]

Paper Information

Journal:   ARCHIVES OF IRANIAN MEDICINE   JULY 2013 , Volume 16 , Number 7; Page(s) 424 To 427.
 
Paper: 

CASE REPORT: HYPOCELLULAR/LYMPHOHISTIOCYTIC VARIANT OF ANAPLASTIC LARGE CELL LYMPHOMA OF LYMPH NODE, MIMICKING GRANULATION TISSUE

 
 
Author(s):  KOSARI FARID*, SAFFAR HIVA, IIZADI BABAK
 
* DEPARTMENT OF PATHOLOGY, SHARIATI HOPITAL, TEHRAN UNIVERSITY OF MEDICAL SCIENCES, TEHRAN, IRAN
 
Abstract: 

Anaplastic Large Cell Lymphoma (ALCL) is a subgroup of T/null cell non-Hodgkin lymphoma (NHL) in WHO classification. Lymphohistiocytic (LH) variant constitutes about 10% of all ALCLs and characterized by presence of abundant reactive histiocytes that can mask the neoplastic nature of the lesion, leading to misdiagnose as “reactive lymphadenopathy”. Here we introduce a 16-year-old female patient, diagnosed as hypocellular LH variant ALCL with unusual histologic feature including granulation tissue- like appearance. We emphasize that in young patients with unusual- looking reactive lymphadenopathy, ALCL should be considered as one of differential diagnoses. A brief review of the nature of the lesion and differential diagnoses is also included.

 
Keyword(s): ANAPLASTIC LARGE CELL LYMPHOMA, HYPOCELLULAR, LYMPHOHISTIOCYTIC VARIANT, REACTIVE LYMPHADENOPATHY
 
References: 
  • ندارد
 
  pdf-File tarjomyar Yearly Visit 97
 
Latest on Blog
Enter SID Blog