Results 261 to 270 of about 340,819 (312)
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Pregnancy and sarcoma

Acta Obstetricia et Gynecologica Scandinavica, 1978
Abstract. Six cases of pregnancy associated with sarcoma are presented. Among these six cases is one patient with vulvar sarcoma which was diagnosed during the 34th week of pregnancy. The literature was reviewed with reference to the effect which pregnancy may have on the growth of malignant tumors.
K, Jafari, A F, Lash, A, Webster
openaire   +2 more sources

Lymphotropic Sarcomas (Epithelioid Sarcoma and Clear Cell Sarcoma)

DeckerMed Complex General Surgical Oncology, 2019
Lymphotropic sarcomas encompass a rare subset of soft tissue sarcoma histotypes known for their distinct ability to metastasize to locoregional lymph nodes. Epithelioid and clear cell sarcomas are the predominant lymphotropic subtypes and the focus of this review. The utility of lymph node assessment, whether clinical, radiographic, and/or surgical, in
Kenneth Cardona   +1 more
openaire   +1 more source

Histiocytic Sarcomas

Leukemia & Lymphoma, 1995
In this study a review of malignancies classified as histiocytic in the literature is given. The available data suggest that a distinction can be made between three main categories, i.e., follicular dendritic cell (FDC) sarcomas, Langerhans' cell/interdigiting reticulum cell (LC/IRC) sarcomas and histiocytic sarcomas (HS) which are unrelated to ...
A F, Lauritzen, E, Ralfkiaer
openaire   +2 more sources

Sarcomas in the Elderly

Clinics in Geriatric Medicine, 1987
Though rare, osteosarcomas and soft tissue sarcomas do occur in the geriatric population. When possible, surgical excision is the treatment of choice, with radiation therapy and chemotherapy having largely an adjuvant role. Classic Kaposi's sarcoma is a chronically progressive and ultimately fatal disease of the elderly which can be managed effectively
A A, Hertler, J O, Moore
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Sarcomas of the Breast

JAMA: The Journal of the American Medical Association, 1967
The term, sarcoma of the breast, without any further qualifications can be misleading because it has been applied to a miscellaneous spectrum of lesions which vary not only in their histologic characteristics but also in clinical behavior. For instance, if in a survey of "sarcoma" of the breast, one should include all cases diagnosed as cystosarcoma ...
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Cutaneous Sarcomas

Hematology/Oncology Clinics of North America, 2019
Cutaneous sarcomas are rare malignancies that may present with a variety of clinical manifestations. This article focuses on 4 of the most common cutaneous sarcomas (Kaposi sarcoma, cutaneous angiosarcoma, dermatofibrosarcoma protuberans, and cutaneous leiomyosarcoma) and reviews clinical, diagnostic, and therapeutic aspects of these rare skin ...
Mehul D, Bhatt, Vinod E, Nambudiri
openaire   +2 more sources

Sarcomas of the heart

Irish Journal of Medical Science, 1986
Primary sarcomas of the heart are fortunately very rare. They may imitate a variety of other cardiac diseases. Despite the great advances in cardiac surgery over the past 20 years, operative intervention in these tumours is only palliative and the prognosis remains very poor.
T, Aherne, M F, Sturridge, K M, Shaw
openaire   +2 more sources

Sarcomas of the breast

Expert Review of Anticancer Therapy, 2012
Sarcomas of the breast are a rare group of heterogeneous mesenchymal tumors accounting for less than 1% of all breast malignancies. Owing to the rarity of the disease, current knowledge is mostly based on numerous case reports and relatively small retrospective series; unlike epithelial breast cancer, there is no high level evidence to support a ...
Guy, Lahat   +5 more
openaire   +2 more sources

Bone Sarcomas

Acta Oncologica, 1996
The literature on radiotherapy for sarcomas originating in bone is limited, and the disease is uncommon. Consequently, this review is based on only 28 scientific articles, including 6 randomized studies, I prospective study, and II retrospective studies. These studies involve 1,394 patients.
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Uterine Sarcoma

Radiology, 1975
Thirty-four cases of uterine sarcoma were studied with regard to their pathologic characteristics and response to treatment. Pathologic features did not always correlate with subsequent course. Combined therapy seems to enhance two-year survival in endometrial stromal sarcoma (ESS), although some patients may have low-grade tumors and hence represent a
R, Belgrad, N, Elbadawi, P, Rubin
openaire   +2 more sources

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