Annals
Established in 1927 by the American College of Physicians
:
Advanced search
box Article
 arrow  Table of Contents                
space
 arrow  Full Text of this article Free
space
 arrow  PDF of this article
space
 arrow  Figures/Tables List
space
box Services
 arrow  Send comment/rapid response letter
space
 arrow  Notify a friend about this article
space
 arrow  Alert me when this article is cited
space
 arrow  Add to Personal Archive
space
 arrow  Download to Citation Manager
space
 arrow  ACP Search
space
 arrow  Get Permissions
space
box Google Scholar
 arrow  Search for Related Content
space
box Social Bookmarking
 Add to CiteULike Add to Complore Add to Connotea Add to Del.icio.us Add to Digg Add to Facebook Add to Reddit Add to Technorati Add to Twitter
What's this?
box PubMed
Articles in PubMed by Author:
 arrow  Cabanillas, F.
space
 arrow  Duvic, M.
space
 arrow  Related Articles in PubMed
space
 arrow  PubMed Citation
space
 arrow  PubMed
space

CLINICAL REVIEW

Lymphomatoid Papulosis: A T-Cell Dyscrasia with a Propensity To Transform into Malignant Lymphoma

right arrow Fernando Cabanillas; James Armitage; William C. Pugh; Dennis Weisenburger; and Madeleine Duvic

1 February 1995 | Volume 122 Issue 3 | Pages 210-217

Objective: To describe the diagnostic difficulties, response to therapy, and clinical features of lymphomatoid papulosis and the cumulative frequency of transformation to lymphoma.

Design: Case series.

Setting: University hospitals.

Methods: The records of 21 patients with lymphomatoid papulosis who were seen from 1986 to 1993 were retrieved from the archives of two institutions. The entry criteria for the study were lymphomatoid papulosis misdiagnosed at the time of original presentation or lymphomatoid papulosis that later developed into lymphoma.

Results: When lymphomatoid papulosis tissues are pathologically examined, they are frequently confused with lymphoma, melanoma, or carcinoma. Eight of the 19 patients whose condition was misdiagnosed as malignant received either chemotherapy or radiotherapy. Although lymphomatoid papulosis responded to cytotoxic chemotherapy, the remissions were transient and promptly recurred after or during treatment. However, all five cases that became malignant responded to chemotherapy and have not recurred. Five of 21 patients (24%) developed lymphoma, but the cumulative risk for transformation after 15 years was 80%.

Conclusions: Lymphomatoid papulosis can only be diagnosed accurately through a careful history in which the characteristic waxing and waning of the skin lesions is identified and through proper communication between clinicians and pathologists. Patients with lymphomatoid papulosis have an increased risk for developing lymphoma that is much higher than the 15% to 20% quoted in the literature. Patients who develop lymphoma respond well to cytotoxic chemotherapy and can be cured with appropriate therapy. Internists and oncologists need to be aware of lymphomatoid papulosis and its characteristic clinical features so that this disorder is accurately diagnosed and so that unnecessary and potentially hazardous treatment is avoided.

Author and Article Information
space

From The University of Texas M.D. Anderson Cancer Center, Houston, Texas; and the University of Nebraska Medical Center, Omaha, Nebraska.
Requests for Reprints: Fernando Cabanillas, MD, Department of Hematology, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard (Box 068), Houston, TX 77030.

 

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
The OncologistHome page
R. Gruber, N. T. Sepp, P. O. Fritsch, and M. Schmuth
Prognosis of Lymphomatoid Papulosis
Oncologist, September 1, 2006; 11(8): 955 - 957.
[Full Text] [PDF]


Home page
The OncologistHome page
E. Jacobsen
Anaplastic Large-Cell Lymphoma, T-/Null-Cell Type
Oncologist, July 1, 2006; 11(7): 831 - 840.
[Abstract] [Full Text] [PDF]


Home page
Cancer Epidemiol. Biomarkers Prev.Home page
M. Franchina, M. E. Kadin, and L. J. Abraham
Polymorphism of the CD30 Promoter Microsatellite Repressive Element Is Associated with Development of Primary Cutaneous Lymphoproliferative Disorders
Cancer Epidemiol. Biomarkers Prev., May 1, 2005; 14(5): 1322 - 1325.
[Abstract] [Full Text] [PDF]


Home page
The OncologistHome page
J. R. Brown and A. T. Skarin
Clinical Mimics of Lymphoma
Oncologist, July 1, 2004; 9(4): 406 - 416.
[Abstract] [Full Text] [PDF]


Home page
Arch DermatolHome page
T. Nijsten, C. Curiel-Lewandrowski, and M. E. Kadin
Lymphomatoid Papulosis in Children: A Retrospective Cohort Study of 35 Cases
Arch Dermatol, March 1, 2004; 140(3): 306 - 312.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
A. Younes and M. E. Kadin
Emerging Applications of the Tumor Necrosis Factor Family of Ligands and Receptors in Cancer Therapy
J. Clin. Oncol., September 15, 2003; 21(18): 3526 - 3534.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
W. Kempf, M. E. Kadin, A. M. Dvorak, C. C. Lord, G. Burg, N. L. Letvin, and I. J. Koralnik
Endogenous retroviral elements, but not exogenous retroviruses, are detected in CD30-positive lymphoproliferative disorders of the skin
Carcinogenesis, February 1, 2003; 24(2): 301 - 306.
[Full Text] [PDF]


Home page
Ann OncolHome page
C. Visco, L. J. Medeiros, D. Jones, T. Smith, M. A. Rodriguez, P. McLaughlin, J. Romaguera, F. Cabanillas, and A. H. Sarris
Primary cutaneous non-Hodgkin's lymphoma with aggressive histology: inferior outcome is associated with peripheral T-cell type and elevated lactate dehydrogenase, but not extent of cutaneous involvement
Ann. Onc., August 1, 2002; 13(8): 1290 - 1299.
[Abstract] [Full Text] [PDF]


Home page
Arch DermatolHome page
T. W. Rozycki and M. D. P. Davis
Recurrent Pruritic Papules in a 74-Year-Old Man
Arch Dermatol, October 1, 2001; 137(10): 1367 - 1372.
[Full Text] [PDF]


Home page
JCOHome page
A. H. Sarris, I. Braunschweig, L. J. Medeiros, M. Duvic, C. S. Ha, M. A. Rodriguez, F. B. Hagemeister, P. McLaughlin, J. Romaguera, J. Cox, et al.
Primary Cutaneous Non-Hodgkin's Lymphoma of Ann Arbor Stage I: Preferential Cutaneous Relapses but High Cure Rate With Doxorubicin-Based Therapy
J. Clin. Oncol., January 15, 2001; 19(2): 398 - 405.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
R. S. Siegel, T. Pandolfino, J. Guitart, S. Rosen, and T. M. Kuzel
Primary Cutaneous T-Cell Lymphoma: Review and Current Concepts
J. Clin. Oncol., August 15, 2000; 18(15): 2908 - 2925.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
M. W. Bekkenk, F. A. M. J. Geelen, P. C. v. V. Vader, F. Heule, M.-L. Geerts, W. A. van Vloten, C. J. L. M. Meijer, and R. Willemze
Primary and secondary cutaneous CD30+ lymphoproliferative disorders: a report from the Dutch Cutaneous Lymphoma Group on the long-term follow-up data of 219 patients and guidelines for diagnosis and treatment
Blood, June 15, 2000; 95(12): 3653 - 3661.
[Abstract] [Full Text] [PDF]


Home page
Journal Watch DermatologyHome page
Lymphomatoid Papulosis Has a High Risk of Transforming into Lymphoma
Journal Watch Dermatology, April 1, 1995; 1995(401): 11 - 11.
[Full Text]




 Home | Current Issue | Past Issues | In the Clinic | ACP Journal Club | CME | Collections | Audio/Video | Mobile | Subscribe | Tools | Help | ACP Online 

Copyright © 1995 by the American College of Physicians.