Reticulum cell sarcoma: Difference between revisions

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{{SK}}Histiocytic lymphoma, histiocytic lymphosarcoma
{{SK}}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:
*[[Ewing's sarcoma]]
*[[Fibrosarcoma]]
*[[Malignant Fibrous Histiocytoma]]
*[[Metastatic carcinoma]]
*[[Osteomyelitis]]
==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===
*[[Radiation therapy]] plus [[chemotherapy]]





Revision as of 13:07, 21 September 2012