Results 121 to 130 of about 4,468 (161)

Dermatofibrosarcoma Protuberans

International Journal of Dermatology, 1984
ABSTRACT: In view of the important clinicopathologic, evolutional, and ultrastructural characteristics of dermatofibrosarcoma Protuberans, a review was made of 30 patients seen during the last 25 years in Colombia's Instituto Nacional de Cancerologia.
G, Gutiérrez, J E, Ospina, N E, de Baez, E K, de Escorcia, R, Gutiérrez   +4 more
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Dermatofibrosarcoma Protuberans

The Journal of Dermatologic Surgery and Oncology, 1988
Abstract. We report the case a 69‐year‐old woman with dermatofibrosarcoma protuberans, present, apparently, since birth. To our knowledge, this case represents the longest reported duration of a dermatofibrosarcoma protuberans.
P J, Weber, J C, Gretzula, O, Hevia, L B, Garland, P, Barquin, E, Gould   +5 more
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Dermatofibrosarcoma Protuberans in Children

Current Treatment Options in Oncology, 2022
Paediatric dermatofibrosarcoma protuberans (DFSP) is a rare soft tissue malignant tumour which displays aggressive local behaviour and has low metastatic potential. The diagnosis is often delayed as DFSP is usually mistaken for other skin conditions, particularly in the early stages of disease.
Aseel Sleiwah, Thomas C. Wright, Thomas Chapman, Adam Dangoor, Francesca Maggiani, Rachel Clancy   +5 more
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Dermatofibrosarcoma Protuberans of the Breast

Tumori Journal, 2008
Background Dermatofibrosarcoma protuberans is an uncommon, locally aggressive but rarely metastasizing tumor of the deep dermis and subcutaneous tissue. It may occur at almost any site but is most common in the trunk and extremities. Dermatofibrosarcoma protuberans of the breast has been rarely reported.
Jong-Yueh Lin, Shyr-Ming Sheen-Chen, Wayne Hsu, Chao-Cheng Huang, Sheung-Fat Ko, Hock-Liew Eng   +5 more
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Congenital Dermatofibrosarcoma Protuberans

Pediatric Dermatology, 1993
Abstract: Congenital dermatofibrosarcoma protuberans occurred in a 16‐year‐old girl. The lesion was a hard cutaneous plaque on the abdomen. It was present at birth and slowly enlarged during the patient's lifetime. Histologic examination was essential to establish the diagnosis and to differentiate it from other congenital fibrohistiocytic ...
Annessi G, Cimitan A, GIROLOMONI, Giampiero, Giannetti A.   +3 more
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Dermatofibrosarcoma protuberans of the vulva

Gynecologic Oncology, 1983
An unusual case of vulvar sarcoma, histologically identified as dermatofibrosarcoma protuberans, is presented together with a summary of current information regarding this lesion.
R, Agress, D C, Figge, H, Tamimi, B, Greer   +3 more
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[Dermatofibrosarcoma: Management].

Bulletin du cancer, 2018
Dematofibrosarcoma protuberans (DFSP) are very rare (1 to 4 incident cases per million of inhabitants). The local spreading of DFSP is underestimated. The histological diagnosis is challenging but we now know a specific marker (translocation t(17;22)(q22;q13) (COL1A1;PDGFB)). The risk of metastatic relapse is low (and related to fibrosarcoma component);
Penel, Nicolas, El Bedoui, Sophie, Robin, Yves-Marie, Decanter, Gauthier   +3 more
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Dermatofibrosarcoma protuberans of the vulva

Acta Obstetricia et Gynecologica Scandinavica, 2004
(2004). Dermatofibrosarcoma protuberans of the vulva. Acta Obstetricia et Gynecologica Scandinavica: Vol. 83, No. 7, pp. 685-686.
Ralf, Ohlinger, Anja, Kühl, Günther, Schwesinger, Petra, Bock, Gerd, Lorenz, Günter, Köhler   +5 more
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Dermatofibrosarcoma protuberans of breast

Cancer Genetics and Cytogenetics, 2003
We describe the case of a 57-year-old woman with a tumor of the breast suspected of being a dermatofibrosarcoma protuberans (DFSP). To confirm the diagnosis, molecular studies were performed on fixed tumor and revealed the presence of the fusion product of the COL1A1-PDGFB genes characteristic of DFSP.
Avery A, Sandberg, William D, Anderson, Christine, Fredenberg, Hiroshi, Hashimoto   +3 more
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Dermatofibrosarcoma Protuberans of the Toe

Annals of Plastic Surgery, 1990
Dermatofibrosarcoma protuberans is an unusual soft-tissue tumor with a propensity for local recurrence and occasional metastatic spread. Given its indolent course, it may be mistaken for atypical scarring or a keloid growth. Most lesions are trunkal or on the proximal extremities with digital lesions being extremely rare.
B A, Kraemer, M, Fremling
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