Reticulum cell sarcoma: Difference between revisions

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*[[Ewing's sarcoma]]
*[[Ewing's sarcoma]]
*[[Fibrosarcoma]]
*[[Fibrosarcoma]]
*[[Malignant Fibrous Histiocytoma]]
*[[Metastatic carcinoma]]
*[[Metastatic carcinoma]]
*[[Osteomyelitis]]
*[[Osteomyelitis]]

Revision as of 23:03, 15 July 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Keywords and synonyms: histiocytic lymphoma, histiocytic lymphosarcoma

Overview

A malignant tumor of reticular tissue in the bone that is composed primarily of neoplastic histocytes.

Pathophysiology

The dominant cell type is thought to be derived from histiocytes or macrophages. More recent thinking indicates that this cancer may arise from lymphocytes or immunoblasts.

Disorders to Distinguish Reticulum Cell Sarcoma From

Epidemiology and Demographics

  • Presents in middle age

Diagnosis

Symptoms

  • Localized bone pain and tenderness

Physical Examination

  • Tenderness of bone
  • Effusion of adjacent joint

Imaging Findings

  • Osteolytic lesions with minimal periosteal reactions are present on plain films of the bone

Pathology

Treatment

Early stage I tumors

Advanced Tumors


References

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