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  2. Liposarcoma - Wikipedia

    en.wikipedia.org/wiki/Liposarcoma

    Since ultrasonography is usually unable to distinguish a liposarcoma from a benign lipoma, MRI is the initial imaging of choice to provide evidence relative to making this distinction. [67] In myxoid liposarcoma, it shows low signal intensity mass with high signal intensity foci on T1-weighted MRI images.

  3. Myxoid liposarcoma - Wikipedia

    en.wikipedia.org/wiki/Myxoid_liposarcoma

    A myxoid liposarcoma is a malignant adipose tissue neoplasm [1] of myxoid appearance histologically.. Myxoid liposarcomas are the second-most common type of liposarcoma, representing 30–40% of all liposarcomas in the limbs, occurring most commonly in the legs, particularly the thigh, followed by the buttocks, retroperitoneum, trunk, ankle, proximal limb girdle, head and neck, and wrist.

  4. Lipoma - Wikipedia

    en.wikipedia.org/wiki/Lipoma

    A lipoma is a benign tumor made of fat tissue. [1] They are generally soft to the touch, movable, and painless. [1] They usually occur just under the skin, but occasionally may be deeper. [1] Most are less than 5 cm (2.0 in) in size. [2] Common locations include upper back, shoulders, and abdomen. [4]

  5. Sarcoma - Wikipedia

    en.wikipedia.org/wiki/Sarcoma

    A sarcoma is a malignant tumor, a type of cancer that arises from cells of mesenchymal (connective tissue) origin. [1] [2] Connective tissue is a broad term that includes bone, cartilage, muscle, fat, vascular, or other structural tissues, and sarcomas can arise in any of these types of tissues.

  6. Soft-tissue sarcoma - Wikipedia

    en.wikipedia.org/wiki/Soft-tissue_sarcoma

    A soft-tissue sarcoma is often a painless mass that grows slowly over months or years. They may be superficial or deep-seated. Any such unexplained mass must be diagnosed by biopsy. [2] Treatment may include surgery, radiotherapy, chemotherapy, and targeted drug therapy. [3] Bone sarcomas are the other class of sarcomas.

  7. Familial multiple lipomatosis - Wikipedia

    en.wikipedia.org/wiki/Familial_Multiple_Lipomatosis

    Familial multiple lipomatosis is a hereditary adipose tissue disorder that is characterized by the formation of multiple lipomas that occur in a particular distribution. [1] The lipomas are well-encapsulated, slow-growing, benign fatty tumors. The distribution is defined as being focused in the trunk of the body and extremities. [2]

  8. File:Histopathology of liposarcoma, annotated.jpg - Wikipedia

    en.wikipedia.org/wiki/File:Histopathology_of_l...

    Date: 18 May 2021: Source: Own work: Author: Mikael Häggström, M.D. Author info - Reusing images - Conflicts of interest: None Mikael Häggström, M.D. Consent note: Consent from the patient or patient's relatives is regarded as redundant, because of absence of identifiable features (List of HIPAA identifiers) in the media and case information (See also HIPAA case reports guidance).

  9. Myxofibrosarcoma - Wikipedia

    en.wikipedia.org/wiki/Myxofibrosarcoma

    Of particular importance, the presence of pseudo-lipoblasts in a myxoid sarcoma-like background is an extremely strong indicator that the tumor is a MFS. [ 6 ] and tumors with a myxofibrosarcoma-like histopathology that initiate in the retroperitoneum, abdominal cavity, or pelvis are nearly always dedifferentiated liposarcomas .