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New England Journal of Medicine, 1962
IN 1872 Kaposi1 described a peculiar pigmented multiple sarcoma of the skin that still defies clinicians and pathologists. Almost 800 cases have been reported in the literature, and many of these have been studied intensively by all methods now available: bacteriologic tests; tissue tests; transplantation; attempted induction by carcinogens ...
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IN 1872 Kaposi1 described a peculiar pigmented multiple sarcoma of the skin that still defies clinicians and pathologists. Almost 800 cases have been reported in the literature, and many of these have been studied intensively by all methods now available: bacteriologic tests; tissue tests; transplantation; attempted induction by carcinogens ...
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Radiotherapy for Kaposi's Sarcoma
The Journal of Dermatologic Surgery and Oncology, 1979Kaposi's sarcoma is a malignancy for which there is no satisfactory standardized, nor even a very good, method of treatment. When the condition is indolent and but slowly progressive on the feet, where it is most common, conservative measures of good local hygiene and palliation of edema, if present, by mechanical support of circulation by elastic ...
T, Borok, A T, Farina, M, Leider
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New England Journal of Medicine, 2020
Penile Kaposi’s Sarcoma A 49-year-old man with human immunodeficiency virus infection presented with ulcerated, violaceous lesions on the penis.
Vieri Grandi, Irene De Francesco
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Penile Kaposi’s Sarcoma A 49-year-old man with human immunodeficiency virus infection presented with ulcerated, violaceous lesions on the penis.
Vieri Grandi, Irene De Francesco
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Clinics in Dermatology, 2001
Before the first clinical descriptions of the acquired immunodeficiency syndrome (AIDS), Kaposi’s sarcoma (KS) was a rare tumor among Western populations, occurring in only 0.02% to 0.06% per 100,000 people.1 In a typical dermatology practice, it was unusual for a busy practitioner to see more than one such case every 5 years. By June and July of 1981,
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Before the first clinical descriptions of the acquired immunodeficiency syndrome (AIDS), Kaposi’s sarcoma (KS) was a rare tumor among Western populations, occurring in only 0.02% to 0.06% per 100,000 people.1 In a typical dermatology practice, it was unusual for a busy practitioner to see more than one such case every 5 years. By June and July of 1981,
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Archives of Ophthalmology, 1978
This report illustrates the clinical and pathological features of epibulbar Kaposi sarcoma in an adult who had no other cutaneous or systemic manifestations of the disorder.
D H, Nicholson, L, Lane
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This report illustrates the clinical and pathological features of epibulbar Kaposi sarcoma in an adult who had no other cutaneous or systemic manifestations of the disorder.
D H, Nicholson, L, Lane
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Radiotherapy of Kaposi's sarcoma
Cancer, 1978Between 1958 and 1976, 34 patients with Kaposi's sarcoma were seen. Two patients were kidney transplant recipients. Co-existing malignancies were seen in 22% of patients. From 1958 to 1965, cutaneous lesions were treated solely with local radiotherapy techniques, single doses of 800 rads being found adequate to produce a complete response.
M J, Holecek, A R, Harwood
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Current Opinion in Oncology, 2003
Knowledge of the pathophysiology of Kaposi sarcoma continues to expand and influence our therapeutic approaches. This review summarizes developments within the last 18 to 24 months.Pieces of the puzzle as they relate to viral factors-both human herpes virus 8 (HHV-8) and human immunodeficiency virus (HIV)-endothelial cells, host immune factors, and ...
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Knowledge of the pathophysiology of Kaposi sarcoma continues to expand and influence our therapeutic approaches. This review summarizes developments within the last 18 to 24 months.Pieces of the puzzle as they relate to viral factors-both human herpes virus 8 (HHV-8) and human immunodeficiency virus (HIV)-endothelial cells, host immune factors, and ...
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Dermatologic Clinics, 1997
KS remains a challenge to clinicians and investigators more than a century after its initial description. Debate continues as to the cell of origin, as well as whether or not it is a true cancer. KS appears to be an opportunistic neoplasm, which in its earliest phase retains some features of a benign hyperproliferative process, but in its late stages ...
P L, Myskowski, R, Ahkami
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KS remains a challenge to clinicians and investigators more than a century after its initial description. Debate continues as to the cell of origin, as well as whether or not it is a true cancer. KS appears to be an opportunistic neoplasm, which in its earliest phase retains some features of a benign hyperproliferative process, but in its late stages ...
P L, Myskowski, R, Ahkami
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Dermatologic Clinics, 1994
The optimal therapy of Kaposi’s Sarcoma (KS) in the setting of AIDS is still to be determined; however, it is fair to say that there is no curative therapy for AIDS-KS, and despite the widespread use of antiviral therapy with zidovudine (azidothymidine), it has been found to be of no benefit in controlling the extent of KS or on restoring the immune ...
P, Gascón, R A, Schwartz
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The optimal therapy of Kaposi’s Sarcoma (KS) in the setting of AIDS is still to be determined; however, it is fair to say that there is no curative therapy for AIDS-KS, and despite the widespread use of antiviral therapy with zidovudine (azidothymidine), it has been found to be of no benefit in controlling the extent of KS or on restoring the immune ...
P, Gascón, R A, Schwartz
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British Journal of Dermatology, 1979
Kaposi's sarcoma occuring in a mother and son is described, and previous reports of familial occurrence of this disease are reviewed.
A Y, Finlay, R, Marks
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Kaposi's sarcoma occuring in a mother and son is described, and previous reports of familial occurrence of this disease are reviewed.
A Y, Finlay, R, Marks
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