“Sarcomas (Sarcomatas)”  

Sarcoma

  In our body, Sarcomas (Sarcomatas), a major histological cancer category, that are aggressive connective and soft tissue neoplasms, originating in connective and supportive tissues such as bones, tendons, cartilage, muscle, and fat, formed by proliferation of mesodermal cells.
  In our body, Sarcoma tumors, usually resemble the tissue in which they grow, mostly occur in young adults, often developing a painful mass located on the bone.
  Examples of sarcomas include:

adenosarcoma carcinosarcoma chondrosarcomas (cartilage sarcomas) mesenchymal chondrosarcoma desmoplastic small round cell tumor endometrial stromal tumors endometrial stromal sarcoma fibrosarcoma dermatofibrosarcoma neurofibrosarcoma hemangiosarcoma lymphosarcoma soft tissue sarcomas malignant fibrous histiocytoma synovial sarcoma

leiomyosarcomas (smooth muscle sarcomas) liposarcoma dedifferentiated liposarcoma pleomorphic liposarcoma lymphangiosarcoma (malignant lymphangioendothelioma) mesodermal mixed tumor myosarcoma rhabdomyosarcomas (skeletal muscle sarcomas) myxosarcoma osteosarcomas (bone sarcomas) Ewing's sarcoma juxtacortical osteosarcoma OSLAM syndrome Phyllodes Tumor alveolar soft part sarcoma clear cell sarcoma Kaposi sarcoma myeloid sarcoma Small Cell Sarcoma Experimental Sarcomas

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“Adenosarcomas”  

  In our body, Adenosarcomas is a malignant neoplasm arising simultaneously or consecutively in mesodermal tissue and glandular epithelium of the same tissue. **

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“Carcinosarcoma”  

  In our body, Carcinosarcoma is a malignant mixed neoplasm that contains intermixed elements of both carcinoma and sarcoma. **

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“Chondrosarcoma”  

Chondrosarcoma (malignant)

  In our body, the sarcoma, Chondrosarcoma is a slow growing malignant connective tissue neoplasm derived from cartilage cells, occurring most frequently in pelvic bones or near the ends of long bones, associated with the CSAG1 gene.
  In our body, the dis-ease, most chondrosarcoma (cartilage sarcoma) arise de novo, but some may develop in a preexisting benign cartilaginous lesion or associated with an enchondromatosis.
  Examples of chondrosarcoma & related cartilage sarcoma dis-orders include:

• mesenchymal chondrosarcoma

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“Desmoplastic Small Round Cell Tumor”  

  In our body, Desmoplastic Small Round Cell Tumor is a rare, aggressive soft tissue sarcoma that primarily affects adolescents and young adults, indicative to a specific set of signs, symptoms or other health indicators, associated with a health challenge most commonly found in the abdomen. **

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“Hemangiosarcoma”  

  In our body, Hemangiosarcoma, an angiosarcoma, is a rare malignant vascular tissue tumor originating from the endothelial cells that line the blood vessel walls.
  In our body, Hemangiosarcoma is characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. **

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“Soft Tissue Sarcomas”  

Soft Tissue Sarcoma

  In our body, Soft Tissue Sarcoma is a malignant soft tissue neoplasm involving a sarcoma, originating in connective and supportive tissues, formed by proliferation of mesodermal cells.
  Examples of subsets, concepts, subjects and related entities of soft tissue sarcomas include:

Adult Soft Tissue Sarcoma Childhood Soft Tissue Sarcoma Alveolar Soft Part Sarcoma Bladder Sarcoma Breast Sarcoma Cardiac Sarcoma Central Nervous System Sarcoma Cervical Leiomyosarcoma Cervical Malignant Peripheral Nerve Sheath Tumor Cervical Rhabdomyosarcoma Clear Cell Sarcoma of Soft Tissue Conjunctival Sarcoma Desmoplastic Small Round Cell Tumor Digestive System Sarcoma Epithelioid Sarcoma Extraskeletal Ewing Sarcoma Extraskeletal Myxoid Chondrosarcoma Extraskeletal Osteosarcoma Fallopian Tube Leiomyosarcoma Intimal Sarcoma Kidney Sarcoma Laryngeal Soft Tissue Sarcoma Leiomyosarcoma of Deep Soft Tissue Localized Soft Tissue Sarcoma Lung Sarcoma Major Salivary Gland Sarcoma Mediastinal Sarcoma Metastatic Soft Tissue Sarcoma Myxosarcoma Oral Cavity Soft Tissue Sarcoma

Orbit Sarcoma Ovarian Sarcoma Paratesticular Leiomyosarcoma Paratesticular Liposarcoma Paratesticular Rhabdomyosarcoma Penile Sarcoma Pericardial Sarcoma Prostate Sarcoma Recurrent Soft Tissue Sarcoma Refractory Soft Tissue Sarcoma Resectable Soft Tissue Sarcoma Retroperitoneal Sarcoma Scrotal Sarcoma Seminal Vesicle Leiomyosarcoma Sinonasal Sarcoma Skin Sarcoma Soft Tissue Angiosarcoma Soft Tissue Fibrosarcoma Soft Tissue Sarcoma of the Trunk and Extremities Stromal Sarcoma Synovial Chondrosarcoma synovial sarcoma Testicular Sarcoma Thyroid Gland Sarcoma Tracheal Sarcoma Undifferentiated Soft Tissue Sarcoma undifferentiated pleomorphic sarcoma Unresectable Soft Tissue Sarcoma Uterine Corpus Sarcoma Vaginal Sarcoma Virus-Related Sarcoma Vulvar Sarcoma

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“Leiomyosarcoma (LMS)”  

Leiomyosarcoma

  In our body, Leiomyosarcoma is a sarcoma involving a muscle tissue neoplasm containing large spindle cells of smooth muscle, indicative to a specific set of signs, symptoms or other health indicators, associated with aggressive connective tissue neoplasms.
  Examples of leiomyosarcoma related dis-orders include:

• Epithelioid Leiomyosarcoma
• Myxoid Leiomyosarcoma

  Examples of subsets, concepts, subjects and related entities of leiomyosarcoma include:

Adrenal Gland Leiomyosarcoma Adult Leiomyosarcoma Advanced Leiomyosarcoma Advanced Soft Tissue Leiomyosarcoma Anal Leiomyosarcoma Appendix Leiomyosarcoma Atypical Intradermal Smooth Muscle Neoplasm Bladder Leiomyosarcoma Bone Leiomyosarcoma Breast Leiomyosarcoma Broad Ligament Leiomyosarcoma Cardiac Leiomyosarcoma Central Nervous System Leiomyosarcoma Cervical Leiomyosarcoma Childhood Leiomyosarcoma Childhood Small Intestinal Leiomyosarcoma Colon Leiomyosarcoma Colorectal Leiomyosarcoma Congenital Peribronchial Myofibroblastic Tumor Conjunctival Leiomyosarcoma Conventional Leiomyosarcoma Dedifferentiated Leiomyosarcoma Digestive System Leiomyosarcoma EBV-Related Leiomyosarcoma Epithelioid Leiomyosarcoma Esophageal Leiomyosarcoma Extrahepatic Bile Duct Leiomyosarcoma Fallopian Tube Leiomyosarcoma Gallbladder Leiomyosarcoma Gastric Leiomyosarcoma Granular Cell Leiomyosarcoma Hamster Ductus Deferens Leiomyosarcoma Hamster Uterine Leiomyosarcoma Inferior Vena Cava Leiomyosarcoma Inflammatory Leiomyosarcoma Kidney Leiomyosarcoma Laryngeal Leiomyosarcoma Leiomyosarcoma and Endometrial Stromal Sarcoma Leiomyosarcoma of Deep Soft Tissue Leiomyosarcoma of Vessels

Liver Leiomyosarcoma Localized Leiomyosarcoma Locally Advanced Leiomyosarcomas Locally Recurrent Uterine Corpus Leiomyosarcoma Lung Leiomyosarcoma Mediastinal Leiomyosarcoma Metastatic Leiomyosarcoma Metastatic Soft Tissue Leiomyosarcoma Metastatic Uterine Corpus Leiomyosarcoma Myxoid Leiomyosarcoma Non-Cutaneous Leiomyosarcoma Ovarian Dermoid Cyst with Leiomyosarcoma Ovarian Leiomyosarcoma Pancreatic Leiomyosarcoma Paratesticular Leiomyosarcoma Penile Leiomyosarcoma Pleomorphic Leiomyosarcoma Pleural Leiomyosarcoma Prostate Leiomyosarcoma Pulmonary Artery Leiomyosarcoma Pulmonary Vein Leiomyosarcoma Rectal Leiomyosarcoma Recurrent Leiomyosarcoma Refractory Leiomyosarcoma Renal Vein Leiomyosarcoma Resectable Leiomyosarcoma Retroperitoneal Leiomyosarcoma Seminal Vesicle Leiomyosarcoma Sinonasal Leiomyosarcoma Small Intestinal Leiomyosarcoma Superior Vena Cava Leiomyosarcoma Thyroid Gland Leiomyosarcoma Unresectable Leiomyosarcomas Uterine Corpus Epithelioid Leiomyosarcoma Uterine Corpus Leiomyosarcoma Uterine Corpus Leiomyosarcoma and Endometrial Stromal Sarcoma Uterine Corpus Myxoid Leiomyosarcoma Vaginal Leiomyosarcoma Vulvar Leiomyosarcoma Well Differentiated Leiomyosarcoma

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“Liposarcoma”  

  In our body, the sarcoma, Liposarcoma is a malignant adipose tissue tumor derived from primitive or embryonal lipoblastic cells indicative to a specific set of signs, symptoms or other health indicators, usually associated with a rich network of capillaries.
  The liposarcoma can be divided into five histological subtypes depending on the grade of their differentiation:

• well-differentiated
• dedifferentiated liposarcoma
• myxoid
• round cell
• pleomorphic

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“Synovial Sarcoma (Synovialosarcoma)”  

Synovial Sarcoma

  In our body, Synovial Sarcoma, originally called Synovioma, is a common soft tissue sarcoma and a malignant connective tissue neoplasm, arising primarily in the paraarticular regions from tenosynovial tissue of the joint capsules and in synovial cells of tendon sheaths and bursae, indicative to a specific set of signs, symptoms or other health indicators.
  In our body, legs are the most common site of a synovial sarcoma, but the tumor may also occur in the abdominal wall and other trunk muscles, commonly associated as a health challenge in the second and fourth decades of life.
  Synovial sarcoma forms a characteristic biphasic patterns, composed of histologically, two morphologically different types of cells include:

• epithelial cells resembling those of carcinoma
• fibrosarcoma-like spindle cells

Histological variants of synovial sarcoma may be subclassified into:

• biphasic synovial sarcoma
  • biphasic type with distinct epithelial and spindle cell components present in various proportions and patterns
• monophasic synovial sarcoma
  • monophasic spindle cell type with little or no evidence of epithelial differentiation
  • monophasic epithelial type
• poorly differentiated type

Immunohistochemically, both epithelial and spindle cells are reactive with cytokeratin and epithelial membrane antigen, while only the spindle cells are positive for vimentin. **

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“Myosarcoma”  

  In our body, Myosarcoma, aka myosarcoma is a sarcoma involving a malignant muscle tissue neoplasm derived from muscular tissue.
  Examples of related myosarcoma dis-orders include:

leiomyosarcoma

rhabdomyosarcoma

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“Alveolar Soft Part Sarcoma”  

Alveolar Soft-Part Sarcoma

  In our body, Alveolar Soft Part Sarcoma is variety of rare sarcoma having a reticulated fibrous stroma, enclosing groups of sarcoma cells, which resemble epithelial cells, enclosed in alveoli walled with connective tissue, associated as a muscle tissue neoplasm. **

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“Clear Cell Sarcoma (Malignant Melanoma of Soft Parts)”  

Clear Cell Sarcoma

  In our body, the dis-ease, Clear Cell Sarcoma is a sarcoma and a connective tissue neoplasm of the lower extremities and acral regions, intimately bound to tendons as circumscribed but unencapsulated melanin-bearing tumors of neuroectodermal origin. **

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“Kaposi's Sarcoma (Multiple Idiopathic Pigmented Hemangiosarcoma)”  

Kaposi Sarcoma

  In our body, the dis-ease, Kaposi Sarcoma is a sarcoma indicative to a specific set of signs, symptoms or other health indicators, associated with vascular tissue neoplasms.
  In our body, the cancer called Kaposi Sarcoma is an infectious associated disease linked or correlated with at least one infectious pathogen (as a herpesviridae viral infection). **

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“Myeloid Sarcoma (Granulocytic Sarcoma)”  

Myeloid Sarcoma

  In our body, the extramedullary tumor, Myeloid Sarcoma is a type of myeloid leukemia involving an extramedullary tumor of immature myeloid cells or myeloblasts, indicative to a specific set of signs, symptoms or other health indicators, associated with a sarcoma (sarcomata).

Granulocytic Sarcoma

  In our body, Granulocytic Sarcoma is a type of myeloid leukemia usually occurs with or follows the onset of an acute myeloid leukemia (AML), indicative to a specific set of signs, symptoms or other health indicators, associated with a sarcoma (sarcomata). **

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