Extramedullary hematopoiesis causing spinal cord compression in polycythemia vera: A case report and literature review.

Author: AgbetsiviKomivi, CailleteauAxel, GuimasValentine, OllivierLuc, SupiotStéphane

Paper Details 
Original Abstract of the Article :
Extramedullary hematopoiesis (EMH) is a rare cause of spinal cord compression defined as finding hematopoietic elements outside the physiological location in the bone marrow. We report the case of a 70-year-old man with JAK 2 positive myeloproliferative syndrome type polycythemia vera (PV), initiall...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638719/

データ提供:米国国立医学図書館(NLM)

Extramedullary Hematopoiesis: A Rare Desert Oasis of Blood Formation

Extramedullary hematopoiesis (EMH) is a rare condition where blood cells are produced outside of the bone marrow, like finding a hidden oasis of life in the middle of a desert. This case report describes a patient with polycythemia vera, a blood disorder, who developed EMH causing spinal cord compression.

A Hidden Oasis: Extramedullary Hematopoiesis

Doctors diagnosed the patient with EMH and successfully treated the spinal cord compression with radiation therapy. This is like discovering the oasis and finding a way to manage the challenges it presents. Radiation therapy, in this case, was a tool to alleviate the pressure on the spinal cord.

The Journey Continues: Managing EMH in Polycythemia Vera

This case report sheds light on the challenges of managing EMH in patients with polycythemia vera. It highlights the importance of careful monitoring and prompt intervention to address the complications associated with this condition.

Dr. Camel's Conclusion

EMH, a rare and often challenging condition, is like a hidden oasis in the desert of blood cell production. By understanding its complexities and developing effective treatment strategies, we can help patients navigate this challenging terrain.

Date :
  1. Date Completed n.d.
  2. Date Revised 2022-11-11
Further Info :

Pubmed ID

36353654

DOI: Digital Object Identifier

PMC9638719

SNS
PICO Info
in preparation
Languages

English

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