Jai Kumar Chaurasia
Dr Lal PathLabs, India
Aligarh Muslim University, India
Scientific Tracks Abstracts: J Cytol Histol
Histiocytic disorders encompasses a number of distinctive entities, arising from histiocytic proliferation ranging from benign, selfresolving lesions to malignant, life-threatening histiocyte rich leukemias and sarcomas. Histiocytes are derived from stem cell precursors in bone marrow from macrophages which later undergo differentiation in various organs to form histiocytes, which are part of the mononuclear phagocytic system. Cytology plays a pivotal role in diagnosing histiocytic disorders, leading to early diagnosis with implications regarding prognosis and treatment. Here, we discuss an interesting case of Rosai-Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy with detailed discussion of differential diagnosis encompassing other histiocytic disorders such as Langerhans cell histiocytosis, hemophagocytic lymphohistiocytosis, xanthogranulomatous lymphohistiocytosis, reactive sinus histiocytosis and histiocyte rich lymphomas and tuberculosis. Rosai-Dorfman disease is a rare non-neoplastic, selflimiting histiocytic proliferative disorder of unknown etiology that usually presents with painless bilateral cervical lymphadenopathy and show distinct cytological features. Retroperitoneal lymph node enlargement due to Rosai-Dorfman disease is unusual and is rarely reported in literature. It is a difficult diagnosis due to disease├ó┬?┬?s non-specific clinical, hematological and radiological findings, often overlapping with other histiocytic disorders. We here discuss an unusual case of Rosai-Dorfman disease in male patient who presented with diffuse abdominal pain and retroperitoneal lymphadenopathy and diagnosed on fine-needle aspiration cytology. This presentation emphasizes that histiocytic disorders should always be dealt with great care and FNAC can be used as a reliable tool to establish the diagnosis, avoiding unnecessary excisional biopsy, aggressive intervention and overtreatment.
Jai Kumar Chaurasia has completed his MD in Pathology from Jawaharlal Nehru Medical College, Aligarh Muslim University (AMU) in India in 2011 and has acquired experience in Pathology from the same institute for three years after completing MD. He is currently working with Dr Lal PathLabs as a Chief of Lab. He has many publications in journals of national and international repute such as Diagnostic Cytopathology (DC), British Medical Journal (BMJ), Journal of Cancer Research and Therapeutics (JCRT) and Indian Journal of Applied Research etc. He is also serving as Reviewer in journals like British Medical Journal and Annals of Medicine and Surgery. He is a Member of Oxford databases as Reviewer.
Email: [email protected]
Journal of Cytology & Histology received 1837 citations as per Google Scholar report