مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

INDETERMINATE CELL HISTIOCYTOSIS: REPORT OF A CASE

Pages

  788-790

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.

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    Cite

    APA: Copy

    GHANADAN, ALIREZA, KAMYAB, KAMBIZ, RAMEZANI, MAZAHER, GOODARZI, AZADEH, DANESHPAZHOOH, MARYAM, BALIGHI, KAMRAN, ANSARI, MAHSA, MIRFALLAH NASSIRI, SEYED FARZAD, & DAKLAN, SOROUSH. (2014). INDETERMINATE CELL HISTIOCYTOSIS: REPORT OF A CASE. ACTA MEDICA IRANICA, 52(10), 788-790. SID. https://sid.ir/paper/278622/en

    Vancouver: Copy

    GHANADAN ALIREZA, KAMYAB KAMBIZ, RAMEZANI MAZAHER, GOODARZI AZADEH, DANESHPAZHOOH MARYAM, BALIGHI KAMRAN, ANSARI MAHSA, MIRFALLAH NASSIRI SEYED FARZAD, DAKLAN SOROUSH. INDETERMINATE CELL HISTIOCYTOSIS: REPORT OF A CASE. ACTA MEDICA IRANICA[Internet]. 2014;52(10):788-790. Available from: https://sid.ir/paper/278622/en

    IEEE: Copy

    ALIREZA GHANADAN, KAMBIZ KAMYAB, MAZAHER RAMEZANI, AZADEH GOODARZI, MARYAM DANESHPAZHOOH, KAMRAN BALIGHI, MAHSA ANSARI, SEYED FARZAD MIRFALLAH NASSIRI, and SOROUSH DAKLAN, “INDETERMINATE CELL HISTIOCYTOSIS: REPORT OF A CASE,” ACTA MEDICA IRANICA, vol. 52, no. 10, pp. 788–790, 2014, [Online]. Available: https://sid.ir/paper/278622/en

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