Reticulum cell sarcoma: Difference between revisions
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{{CMG}} | {{CMG}} | ||
{{SK}} | {{SK}}Histiocytic lymphoma, histiocytic lymphosarcoma | ||
==Overview== | ==Overview== | ||
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*[[Radiation therapy]] plus [[chemotherapy]] | *[[Radiation therapy]] plus [[chemotherapy]] | ||
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[[Category:Hematology]] | [[Category:Hematology]] | ||
Revision as of 12:57, 21 September 2012
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Reticulum cell sarcoma Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Reticulum cell sarcoma On the Web |
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American Roentgen Ray Society Images of Reticulum cell sarcoma |
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Risk calculators and risk factors for Reticulum cell sarcoma |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: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.
Differentiating Reticulum Cell Sarcoma From Other Diseases
Reticulum cell sarcoma should be distinguished from the following diseases:
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
- Large, foam filled histiocytes with numerous mitoses and scant stroma are present
- Stains for reticulum are positive
- Periodic Acid Schiff (PAS) stains are negative
Treatment
Early stage I tumors
- Radiation therapy alone
Advanced Tumors
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