Paper Information

Journal:   ACTA MEDICA IRANICA   2014 , Volume 52 , Number 10; Page(s) 788 To 790.
 
Paper: 

INDETERMINATE CELL HISTIOCYTOSIS: REPORT OF A CASE

 
Author(s):  GHANADAN ALIREZA, KAMYAB KAMBIZ, RAMEZANI MAZAHER*, GOODARZI AZADEH, DANESHPAZHOOH MARYAM, BALIGHI KAMRAN, ANSARI MAHSA*, MIRFALLAH NASSIRI SEYED FARZAD, DAKLAN SOROUSH
 
* DEPARTMENT OF DERMATOLOGY, RAZI HOSPITAL, TEHRAN UNIVERSITY OF MEDICAL SCIENCES, TEHRAN, IRAN
 
Abstract: 

Indeterminate cell histiocytosis is a very rare disorder of histiocytes proliferation. It has both Langerhans and non-Langerhans cell histiocytosis immunophenotypic features. We described a 45-year-old man with a 2 years history of multiple yellow-brown papules and a few red nodules on his trunk and extremities. No internal involvement was detected first and after 8 months. As his lesions were asymptomatic and sparse, he didn’t receive any treatment. He will be followed at regular intervals.

 
Keyword(s): INDETERMINATE CELL HISTIOCYTOSIS, NON-LANGERHANS CELL HISTIOCYTOSIS, IMMUNOHISTOCHEMISTRY
 
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