Leiomyosarcoma

Leiomyosarcoma

Leiomyosarcoma of the adrenal vein. Coronal view of abdominal MRI. Tumor (arrow) extends from the superior pole of the right kidney to the right atrium.
Classification and external resources
Specialty Hematology and Oncology
ICD-10 C49.M48
ICD-O M8890/3
DiseasesDB 34362
MedlinePlus 000916
eMedicine med/1180
MeSH D007890

Leiomyosarcoma (Gr. "smooth muscle connective tissue tumor"), also referred to as LMS, is a malignant (cancerous) smooth muscle tumor. A benign tumor originating from the same tissue is termed leiomyoma. It is also important to note that leiomyosarcomas do not arise from leiomyomas.[1]

Leiomyosarcoma is a rare form of cancer, and accounts for 5–10% of soft-tissue sarcomas, which are in themselves relatively rare.[2] Leiomyosarcomas can be very unpredictable. They can remain dormant for long periods of time and recur after years. It is a resistant cancer, meaning generally not very responsive to chemotherapy or radiation. The best outcomes occur when it can be removed surgically with wide margins early, while small and still in situ.[3]

Location

Smooth muscle cells make up the involuntary muscles, which are found in most parts of the body, including the uterus, stomach and intestines, the walls of all blood vessels, and the skin. It is therefore possible for leiomyosarcomas to appear at any site in the body. They are most commonly found in the uterus,[4] stomach, small intestine and retroperitoneum.[5]

Uterine leiomyosarcomas come from the smooth muscle in the muscle layer of the uterus.[6] Cutaneous leiomyosarcomas derive from the pilo-erector muscles in the skin. Gastrointestinal leiomyosarcomas might come from smooth muscle in the GI tract or, alternatively, also from a blood vessel. At most other primary sites—retroperitoneal extremity (in the abdomen, behind the intestines), truncal, abdominal organs, etc.—leiomyosarcomas appear to grow from the muscle layer of a blood vessel (the tunica media). Thus a leiomyosarcoma can have a primary site of origin anywhere in the body where there is a blood vessel.[3]

The tumors are usually hemorrhagic and soft and microscopically marked by pleomorphism, abundant (15–30 per 10 high power fields) abnormal mitotic figures, and coagulative tumor cell necrosis. There is a wide differential diagnosis, which includes spindle cell carcinoma, spindle cell melanoma, fibrosarcoma, malignant peripheral nerve sheath tumor and even biphenotypic sinonasal sarcoma.

Treatment

Surgery, with as wide a margin of removal as possible, has generally been the most effective and preferred way to attack LMS. If surgical margins are narrow or not clear of tumor, however, or in some situations where tumor cells were left behind, chemotherapy or radiation has been shown to give a clear survival benefit.[7] While LMS tends to be resistant to radiation and chemotherapy, each case is different and results can vary widely.

LMS of uterine origin do frequently, but not always respond to hormonal treatments.[8][9]

Notable patients

Notable people who have had leiomyosarcoma include:

See also

References

  1. Kumar, Vinay; Abbas, Abul; Aster, Jon (2015). Robbins and Cotran Pathologic Basis of Disease. Philadelphia, PA: Elsevier. pp. 1020–1021. ISBN 978-1-4557-2613-4.
  2. Weaver MJ, Abraham JA (2007). "Leiomyosarcoma of the Bone and Soft Tissue: A Review". ESUN. 4 (2).
  3. 1 2 "Basic info". www.leiomyosarcoma.info. LMS leiomyosarcoma.
  4. Arnold LM, Burman SD, O-Yurvati AH (April 2010). "Diagnosis and management of primary pulmonary leiomyosarcoma". J Am Osteopath Assoc. 110 (4): 244–6. PMID 20430913.
  5. Piovanello P, Viola V, Costa G, et al. (2007). "Locally advanced leiomyosarcoma of the spleen. A case report and review of the literature". World J Surg Oncol. 5 (1): 135. doi:10.1186/1477-7819-5-135. PMC 2221972Freely accessible. PMID 18045454.
  6. Sue Ghosh; Jonathan Hecht; Tanaz Ferzandi,; Christopher Awtrey (2007). "Leiomyosarcoma of the Uterus (ULMS): A Review". The Liddy Shriver Sarcoma Initiative. Retrieved 1 February 2016.
  7. "About Chemotherapy". www.leiomyosarcoma.info. LMS leiomyosarcoma. August 2002.
  8. Abu-Rustum, N. R.; Curtin, J. P.; Burt, M.; Jones, W. B. (1997). "Regression of uterine low-grade smooth-muscle tumors metastatic to the lung after oophorectomy". Obstetrics and gynecology. 89 (5 Pt 2): 850–852. doi:10.1016/S0029-7844(97)00033-1. PMID 9166348.
  9. Hardman, M. P.; Roman, J. J.; Burnett, A. F.; Santin, A. D. (2007). "Metastatic Uterine Leiomyosarcoma Regression Using an Aromatase Inhibitor". Obstetrics & Gynecology. 110 (2 Pt 2): 518–520. doi:10.1097/01.AOG.0000267533.56546.c2. PMID 17666649.
  10. "World's first skull and scalp transplant performed on cancer sufferer with huge hole in head".
  11. "deadline.com".
  12. "pforpadma.org".
  13. "Leicester legend Weller mourned". BBC Online. 2004-11-13. Retrieved 2010-05-14.
  14. "Jordan treated for cancer". BBC Online. 2002-08-11. Retrieved 2009-10-30.
  15. Gillespie, Kerry (2008-04-12). "'Can't ever give up hope,' Basrur says". The Toronto Star. Retrieved 2010-01-08.
  16. "That's My Time". www.irwinbarker.com. Archived from the original on 2008-10-02. Retrieved 5 March 2015. In Irwin's own words: “Cancer has my body but not my spirit, and I'll continue to make jokes, not so much about cancer, but in spite of it.”

External links

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