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Article

Acute Promyelocytic Leukemia, Hypogranular Variant: A Rare Presentation

Department of Pathology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh (UP), India
*
Author to whom correspondence should be addressed.
Clin. Pract. 2011, 1(1), e11; https://doi.org/10.4081/cp.2011.e11
Submission received: 15 March 2011 / Revised: 15 March 2011 / Accepted: 29 March 2011 / Published: 12 April 2011

Abstract

Early diagnosis of acute promyelocytic leukemia (APL) is essential because of its associated life threatening coagulopathy and unique response to all trans-retinoic acid (ATRA) therapy. The characteristic cell morphology supplemented by cytochemistry offers the most rapid means for diagnosis. Here we describe a rare case of acute promyelocytic leukemia-hypogranular variant that poses particular diagnostic challenge.
Keywords: acute promyelocytic leukemia; hypogranular variant; cytochemistry acute promyelocytic leukemia; hypogranular variant; cytochemistry

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MDPI and ACS Style

Akhtar, K.; Ahmad, S.; Sherwani, R.K. Acute Promyelocytic Leukemia, Hypogranular Variant: A Rare Presentation. Clin. Pract. 2011, 1, e11. https://doi.org/10.4081/cp.2011.e11

AMA Style

Akhtar K, Ahmad S, Sherwani RK. Acute Promyelocytic Leukemia, Hypogranular Variant: A Rare Presentation. Clinics and Practice. 2011; 1(1):e11. https://doi.org/10.4081/cp.2011.e11

Chicago/Turabian Style

Akhtar, Kafil, Shamshad Ahmad, and Rana K. Sherwani. 2011. "Acute Promyelocytic Leukemia, Hypogranular Variant: A Rare Presentation" Clinics and Practice 1, no. 1: e11. https://doi.org/10.4081/cp.2011.e11

APA Style

Akhtar, K., Ahmad, S., & Sherwani, R. K. (2011). Acute Promyelocytic Leukemia, Hypogranular Variant: A Rare Presentation. Clinics and Practice, 1(1), e11. https://doi.org/10.4081/cp.2011.e11

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