Polycythemia
Diseases

Author: Gianpiero Pescarmona
Date: 04/09/2011

Description

DEFINITION

The disease definition according to a specific consensus conference or to The Diseases Database based on the Unified Medical Language System (NLM)

Also the link to the corresponding Mesh term has to be created

DatabaseLink
WikipediaFabry
The Diseases DatabaseURL
MedlinePlus"URL":
OMIM single geneFabry
WikigenesAGAL
GeneCards"AGAL":
Kegg PathwayAGAL

Se ci sono piĆ¹ voci su OMIM usare questo formato di ricerca:

Autism

EPIDEMIOLOGY

age, sex, seasonality, etc

SYMPTOMS

DIAGNOSIS

histopathology
radiology
NMR
laboratory tests

PATHOGENESIS

PATIENT RISK FACTORS

Vascular

Genetic

Acquired

Hormonal

Genetic

Acquired

Erythrocytosis caused by an erythropoietin-producing hepatocellular carcinoma. 2000

  • Abstract
    A case of erythrocytosis caused by a hepatocellular carcinoma (HCC) that produced erythropoietin (Epo) is described. A 64-year-old man, with a huge HCC tumor in the right lobe of the liver, showed a high concentration of hemoglobin and increased levels of serum Epo, alpha-fetoprotein (AFP), and protein induced by vitamin K absence II (PIVKA-II). Right lobectomy of the liver was performed. Histological findings of the specimen showed a moderately differentiated HCC. The existence of Epo was confirmed immunohistochemically only in the tumor tissue and not in the normal liver tissue. Erythrocytosis disappeared and the serum levels of Epo, AFP, and PIVKA-II returned to the normal range after the operation. Within 2 months after the operation, recurrent tumors appeared in the remnant liver, and the patient died 13 months after the operation.

TISSUE SPECIFIC RISK FACTORS

anatomical (due its structure)

vascular (due to the local circulation)

physiopathological (due to tissue function and activity)

polycythemia+and+HIF-1a

COMPLICATIONS

THERAPY

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