スチュワート・トリーヴス症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- Scottish philosopher and follower of Thomas Reid (1753-1828) (同)Dugald Stewart
- United States film actor who portrayed incorruptible but modest heros (1908-1997) (同)Jimmy Stewart, James Maitland Stewart
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
- =Stuart
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/05/28 00:35:36」(JST)
[Wiki en表示]
Stewart–Treves syndrome, also known as cutaneous angiosarcoma, refers to a lymphangiosarcoma, a rare complication that forms as a result of chronic, long-standing lymphedema. Although it most commonly refers to malignancies associated with chronic lymphedema resulting from mastectomy and/or radiotherapy for breast cancer,[1] it may also describe lymphangiosarcomas that result from congenital and other causes of chronic secondary lymphedema.[2] Lymphangiosarcoma arising from cancer-related lymphedema has become much less common with better surgical techniques, radiation therapy, and conservative treatment.[3] The prognosis, even with wide surgical excision and subsequent radiotherapy, is poor.[4]
Contents
- 1 History
- 2 Incidence
- 3 Treatment
- 4 Prognosis
- 5 See also
- 6 References
History
It was discovered by Fred W. Stewart and Norman Treves in 1948.
Incidence
In the 1960s, the incidence 5 years after a radical mastectomy varied from 0.07% to 0.45%.[5] Today, it occurs in 0.03% of patients surviving 10 or more years after radical mastectomy.[6]
Treatment
The treatment of choice is a large resection or amputation of the affected limb. Radiation therapy can precede or follow surgical treatment. Tumors that have advanced locally or have metastasized can be treated with mono or polychemotherapy, systemically or locally.[6] However, chemotherapy and radiation therapy have not been shown to improve survivorship significantly.[2]
Prognosis
Early detection is key. Untreated patients usually live 5 to 8 months after diagnosis.[2]
See also
- Lymphangiosarcoma
- Angiosarcoma
- Masectomy
- Postcardiotomy syndrome
- List of cutaneous conditions
- Lymphedema
References
- ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
- ^ a b c Sharma, A; Schwartz, RA (June 2012). "Stewart-Treves syndrome: Pathogenesis and management.". J Am Acad Dermatol 67 (6): 1342–8. doi:10.1016/j.jaad.2012.04.028. PMID 22682884.
- ^ Kumar MBBS MD FRCPath, Vinay (2010). Robins and Cotran: Pathologic Basis of Disease 8th Edition. Philadelphia, PA: Saunders Elsevier. p. 1093. ISBN 978-1-4160-3121-5.
- ^ Pincus LB, Fox LP (August 2008). "Images in clinical medicine. The Stewart-Treves syndrome". N. Engl. J. Med. 359 (9): 950. doi:10.1056/NEJMicm071344. PMID 18753651.
- ^ Heitmann, C; Ingianni, G (January 2000). "Stewart-Treves syndrome: lymphangiosarcoma following mastectomy.". Ann Plast Surg. 44 (1): 72–5. doi:10.1097/00000637-200044010-00012. PMID 10651369.
- ^ a b Wierzbicka-Hainaut, E; Guillet, G (December 2010). "[Stewart-Treves syndrome (angiosarcoma on lyphoedema): A rare complication of lymphoedema]". Presse Med. 39 (12): 1305–8. doi:10.1016/j.lpm.2010.06.017. PMID 20970956.
UpToDate Contents
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English Journal
- Lymphangiosarcoma: Is Stewart-Treves Syndrome a Preventable Condition?
- Felmerer G1, Dowlatshahi AS2,3, Stark GB3, Földi E4, Földi M4, Ahls MG5, Ströbel P5, Aung T1.
- Lymphatic research and biology.Lymphat Res Biol.2015 Nov 19. [Epub ahead of print]
- BACKGROUND: Stewart-Treves syndrome is a rare complication of breast cancer treatment, representing a lymphangiosarcoma commonly associated with lymphedema and severely impacting patient's outcome. The tumor typically develops in the atrophic, pachydermatous, hyperkeratotic skin of limbs affected by
- PMID 26584023
- Lebarbier-Dumesnil A1, Cailleux-Talbot N2, Armengol G2, Lévesque H2, Benhamou Y2.
- La Revue de medecine interne / fondee ... par la Societe nationale francaise de medecine interne.Rev Med Interne.2015 Oct 9. pii: S0248-8663(15)00638-4. doi: 10.1016/j.revmed.2015.09.002. [Epub ahead of print]
- PMID 26460195
- Stewart-Treves Syndrome of the Breast after Quadrantectomy for Breast Carcinoma.
- Miglino B1, Maldi E2, Tiberio R1, Boggio P1, Astolfi S1, Franchini R3, Zavattaro E1, Boldorini R2, Colombo E1.
- The breast journal.Breast J.2015 Sep-Oct;21(5):552-4. doi: 10.1111/tbj.12457. Epub 2015 Jul 23.
- PMID 26205517
Japanese Journal
- 症例 外科的切除を行った下腹部のStewart-Treves症候群の1例
- まれな原因で生じたStewart-Treves症候群の2例
- 日形会誌 : 日本形成外科学会会誌 = Journal of Japan Society of Plastic and Reconstructive Surgery 33(9), 689-696, 2013-09-20
- NAID 10031201594
Related Links
- Stewart-Treves syndromeとは,種々の原因による四肢の慢性のリンパ浮腫を発生母地とした脈管肉腫を主体とした症候群である.これは,1948年にStewartとTrevesが乳房切断術後の慢性リンパ浮腫に生じた脈管肉腫を報告したことに由来 ...
- Stewart-Treves syndrome is a rare, deadly cutaneous angiosarcoma that develops in long-standing chronic lymphedema. [1, 2, 3] Most commonly, this tumor is a result of lymphedema induced by radical mastectomy to treat breast cancer. Unfortunately, although the breast cancer may be cured with such radical surgery ...
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