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botryoid sarcoma |
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sarcoma /sar·co·ma/ (sahr-ko´mah) pl. sarcomas, sarco´mata any of a group of tumors usually arising from connective tissue, although the term now includes some of epithelial origin; most are malignant.
alveolar soft part sarcoma a well-circumscribed, painless, highly metastatic neoplasm with a distinctive alveolar pattern, usually in the limbs, head, and neck of young adults. ameloblastic sarcoma see under fibrosarcoma. botryoid sarcoma , sarcoma botryoi´des an embryonal rhabdomyosarcoma arising in submucosal tissue, usually in the upper vagina, cervix uteri, or neck of urinary bladder in young children and infants, presenting grossly as a polypoid grapelike structure. clear cell sarcoma of kidney a malignant kidney tumor similar to Wilms' tumor but with poorer prognosis, often metastasizing to bone. endometrial stromal sarcoma a pale, polypoid, fleshy, malignant tumor of the endometrial stroma. Ewing's sarcoma a highly malignant, metastatic, primitive small round cell tumor of bone, usually in the diaphyses of long bones, ribs, and flat bones of children and adolescents. giant cell sarcoma 1. a form of giant cell tumor of bone arising malignant de novo rather than transforming to malignancy. 2. sarcoma characterized by large anaplastic (giant) cells. hemangioendothelial sarcoma hemangiosarcoma. immunoblastic sarcoma of B cells large cell immunoblastic lymphoma composed predominantly of B cells. immunoblastic sarcoma of T cells large cell immunoblastic lymphoma composed predominantly of T cells. Kaposi sarcoma a multicentric, malignant neoplastic vascular proliferation, characterized by the development of bluish-red nodules on the skin, sometimes with widespread visceral involvement; a particularly virulent, disseminated form occurs in immunocompromised patients. Kupffer cell sarcoma hepatic angiosarcoma. osteogenic sarcoma osteosarcoma. pseudo–Kaposi sarcoma unilateral subacute to chronic dermatitis occurring in association with an underlying arteriovenous fistula and closely resembling Kaposi's sarcoma clinically and histologically. reticulum cell sarcoma histiocytic lymphoma. Rous sarcoma a virus-induced sarcoma-like growth of fowls. soft tissue sarcoma a general term for a malignant tumor derived from extraskeletal connective tissue, including fibrous, fat, smooth muscle, nerve, vascular, histiocytic, and synovial tissue, with almost all lesions arising from primitive mesoderm. spindle cell sarcoma
1. any sarcoma composed of spindle-shaped cells. 2. a type of soft tissue sarcoma whose cells are spindle-shaped and which is usually resistant to radiation therapy.
sarcoma [sahr-ko´mah] (pl. sarcomas, sarco´mata.) A tumor, often highly malignant, composed of cells derived from connective tissue such as bone, cartilage, muscle, blood vessel, or lymphoid tissue; sarcomas usually develop rapidly and metastasize through the lymph channels. Different types are named for the specific tissue they affect: fibrosarcoma in fibrous connective tissue; lymphosarcoma in lymphoid tissues; osteosarcoma in bone; chondrosarcoma in cartilage; rhabdosarcoma in muscle; and liposarcoma in fat cells. adj., adj sarco´matous. Abernethy's sarcoma a malignant fatty tumor occurring mainly on the trunk. alveolar soft part sarcoma one with a reticulated fibrous stroma enclosing groups of sarcoma cells enclosed in alveoli walled with connective tissue. botryoid sarcoma (sarcoma botryoi´des) an embryonal rhabdomyosarcoma arising in submucosal tissue, usually in the upper vagina, cervix uteri, or bladder neck in young children and infants, presenting grossly as a polypoid grapelike structure. endometrial stromal sarcoma a pale, polypoid, fleshy, malignant tumor of the endometrial stroma. Ewing's sarcoma a malignant tumor of the bone that arises in medullary tissue, usually found in cylindrical bones, with pain, fever, and leukocytosis as prominent symptoms; called also Ewing's tumor. giant cell sarcoma a malignant form of giant cell tumor of bone. granulocytic sarcoma chloroma. immunoblastic sarcoma of B cells an aggressive B-cell lymphoma believed to arise from transformed interfollicular B lymphocytes, which in many cases is associated with a preexisting immunologic disorder, e.g., Sjögren's syndrome, systemic lupus erythematosus, or Hashimoto's thyroiditis, or with an immunocompromised state. immunoblastic sarcoma of T cells a group of T-cell lymphomas comprising tumors derived from T lymphocytes in the paracortical area arising from a mixture of small lymphocytes and many large transformed cells; the latter are characterized by one or more small but distinctly eosinophilic nucleoli. Kaposi sarcoma a multicentric, malignant neoplastic vascular proliferation characterized by bluish red cutaneous nodules, usually on the lower extremities, most often on the toes or feet; the nodules slowly increase in size and number and spread to more proximal sites. Tumors often remain confined to skin and subcutaneous tissue, but widespread visceral involvement may occur. The condition occurs endemically in certain parts of Central Africa and Central and Eastern Europe, and a particularly virulent and disseminated form occurs in immunocompromised patients such as transplant recipients and those with acquired immunodeficiency syndrome. Human herpesvirus 8 has been implicated as a causative agent. lymphatic sarcoma diffuse lymphoma. osteogenic sarcoma a malignant primary tumor of bone composed of a malignant connective tissue stroma with evidence of osteoid, bone, and/or cartilage formation; depending upon the dominant component, classified as osteoblastic, fibroblastic, or chondroblastic. pseudo–Kaposi sarcoma unilateral subacute to chronic dermatitis, often with postinflammatory hyperpigmentation, occurring in association with underlying arteriovenous fistula, which closely resembles Kaposi sarcoma both clinically and histologically. reticulum cell sarcoma histiocytic lymphoma.
botryoid sarcoma Myxoid variant of embryonal rhabdomyosarcoma A tumor of hollow organs–urinary bladder, vagina of children DiffDx Intramuscular myxoma, myxoid liposarcoma, myxoid MFH, botryoid sarcoma–myxoid embryonal
rhabdomyosarcoma Management Excision, chemotherapy, RT Prognosis Poor without aggressive therapy; early metastases Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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