Lymphomatoid papulosis: a clinical and histopathologic review and follow-up study of 34 cases in Taiwan
Background: Lymphomatoid papulosis (LyP) is a rare condition within the spectrum of CD30+ cutaneous lymphoproliferative disorders that is not well documented in Taiwan. This study aimed to analyze its clinical manifestations, diagnostic histopathology, clinical course, and treatment response among T...
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Wolters Kluwer Medknow Publications,
2011-03-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_ba11f6d56b5041a6b55d12c8c124c444 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Jheng-Wei Lin |e author |
700 | 1 | 0 | |a Wen-Jin Shiau |e author |
700 | 1 | 0 | |a Ching-I. Lu |e author |
700 | 1 | 0 | |a Chang-You Tsai |e author |
700 | 1 | 0 | |a Wen-Ron Wong |e author |
700 | 1 | 0 | |a Rosaline Chung-Yee Hui |e author |
245 | 0 | 0 | |a Lymphomatoid papulosis: a clinical and histopathologic review and follow-up study of 34 cases in Taiwan |
260 | |b Wolters Kluwer Medknow Publications, |c 2011-03-01T00:00:00Z. | ||
500 | |a 1027-8117 | ||
500 | |a 10.1016/j.dsi.2011.02.001 | ||
520 | |a Background: Lymphomatoid papulosis (LyP) is a rare condition within the spectrum of CD30+ cutaneous lymphoproliferative disorders that is not well documented in Taiwan. This study aimed to analyze its clinical manifestations, diagnostic histopathology, clinical course, and treatment response among Taiwanese. Methods: A retrospective chart review was performed on patients diagnosed with LyP at a Taiwanese medical center from 1992 to 2008. Results: There were 34 patients with biopsy-proven LyP. The mean age at diagnosis was 36 years (range: 10-75 years), with male predominance (male:female ratio 3:2). Type-A LyP was identified in 32 patients and Type C in 2 patients. Seven cases showed CD4 predominance and six cases showed CD8 predominance. Of the 34 LyP patients, 2 had coexistent non-Hodgkin's lymphoma, 1 (3%, 1/34) diagnosed before LyP onset and 1 (3%, 1/34) developed lymphoma 3 years after LyP. All of the patients were alive after a mean of 5.2 years (range: 3-12.7 years) of follow-up. Conclusions: Most of our cases are Type A LyP. No clinical features or pathologic features can predict increased risk for developing malignancy. Although only 6% (2/34) of LyP patients were found to have lymphoma in 3-year follow-up, longer follow up is needed. Regardless of treatment modalities, two-thirds of the patients have a recurrent and relapsing course. Observation is a reasonable approach for patients without cosmetic or symptomatic concerns. | ||
546 | |a EN | ||
690 | |a Lymphomatoid papulosis | ||
690 | |a Lymphoproliferative disorder | ||
690 | |a Non-Hodgkin's lymphoma | ||
690 | |a Dermatology | ||
690 | |a RL1-803 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Dermatologica Sinica, Vol 29, Iss 1, Pp 8-12 (2011) | |
787 | 0 | |n http://www.sciencedirect.com/science/article/pii/S1027811711000115 | |
787 | 0 | |n https://doaj.org/toc/1027-8117 | |
856 | 4 | 1 | |u https://doaj.org/article/ba11f6d56b5041a6b55d12c8c124c444 |z Connect to this object online. |