2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Neoplasms 140-239 > Malignant Neoplasm Of Lymphatic And Hematopoietic Tissue 200-208 > Other Malignant Neoplasms Of Lymphoid And Histiocytic Tissue 202.* >
 2007 ICD-9-CM Diagnosis 202.3
Malignant histiocytosis On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date.
The 2009 version of ICD-9-CM 202.3 can be accessed here. - A rare, usually rapidly progressive disorder, characterized by abrupt onset, fever, weight loss, hepato-splenomegaly, pancytopenia, and lymphadenopathy.
- An aggressive Non-Hodgkin's adult lymphoma, comprised of two clinical syndromes: nasal T-cell lymphoma (previously called lethal midline granuloma) and pulmonary angiocentric B-cell lymphoma (previously called lymphomatoid granulomatosis). (PDQ)
- 202.3 is a non-specific code that cannot be used to specify a diagnosis
- 202.3 contains 5 index entries
- View the ICD-9-CM Volume 1 202.* hierarchy
202.3 also known as:- Histiocytic medullary reticulosis
- Malignant:
- reticuloendotheliosis
- reticulosis
Index entries containing 202.3:- Histiocytosis (acute) (chronic) (subacute) 277.89
- malignant (M9720/3)
 202.3
Reticuloendotheliosis- malignant (M9720/3) 202.3
Reticulosis (skin)- histiocytic medullary (M9721/3) 202.3
- malignant (M9720/3) 202.3
Sarcoma (M8800/3) - see also Neoplasm, connective tissue, malignant- reticuloendothelial (M9720/3) 202.3
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