Subcutaneous panniculitis-like T-cell lymphoma

Common Name(s)

Subcutaneous panniculitis-like T-cell lymphoma

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Subcutaneous panniculitis-like T-cell lymphoma" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Subcutaneous panniculitis-like T-cell lymphoma" returned 24 free, full-text research articles on human participants. First 3 results:

Subcutaneous panniculitis-like T-cell lymphoma with bone marrow involvement.
 

Author(s): Noah A Brown, Charles W Ross, Johann E Gudjonsson, Daniel Wale, Attaphol Pawarode, Ivan Maillard, Alexandra C Hristov

Journal: Am. J. Clin. Pathol.. 2015 Feb;143(2):265-73.

 

To describe a rare case of subcutaneous panniculitis-like T-cell lymphoma (SPTCL) with morphologic and immunophenotypic evidence of bone marrow involvement.

Last Updated: 17 Jan 2015

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A subcutaneous panniculitis-like T-cell lymphoma mimicking dermatomyositis.
 

Author(s): Shinjiro Kaieda, Akiko Idemoto, Naomi Yoshida, Hiroaki Ida

Journal: Intern. Med.. 2014 ;53(13):1455.

 

Last Updated: 3 Jul 2014

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Subcutaneous panniculitis-like T-cell lymphoma with unusual eschar-like crusting.
 

Author(s): Supid Kumar Ghosh, Debsmita Roy, Priyanker Mondal, Deblina Bhunia, D P Dutta

Journal:

 

Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare subtype of non-Hodgkin's lymphoma of the skin. Clinically, SPTCL presents as subcutaneous tumors located on the extremities or trunk, often associated with systemic symptoms like fever or fatigue. The therapeutic regimen ...

Last Updated: 11 Mar 2014

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Subcutaneous panniculitis-like T-cell lymphoma" returned 2 free, full-text review articles on human participants. First 3 results:

Progressive and painful wound as a feature of subcutaneous panniculitis-like T-cell lymphoma (SPTCL): report of a case and review of literature.
 

Author(s): Qixia Jiang, Yuanling Xu, Xiaohua Li, Qing Peng, Hui Cai, Jiandong Wang

Journal:

 

Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is an uncommon extranodal non-Hodgkin lymphoma, with an aggressive course with no well-defined treatment. This article describes a 56-year-old man, treated surgically 7 months earlier for a subcutaneous nodosity near the left ...

Last Updated: 10 Mar 2015

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Immunophenotypic and molecular features, clinical outcomes, treatments, and prognostic factors associated with subcutaneous panniculitis-like T-cell lymphoma: a systematic analysis of 156 patients reported in the literature.
 

Author(s): Ronald S Go, Susan M Wester

Journal: Cancer. 2004 Sep;101(6):1404-13.

 

Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is an uncommon type of skin lymphoma. The natural history, optimal treatment strategy, and prognostic factors associated with this malignancy are not well defined.

Last Updated: 15 Sep 2004

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

CTOP/ITE/MTX Compared With CHOP as the First-line Therapy for Newly Diagnosed Young Patients With T Cell Lymphoma
 

Status: Recruiting

Condition Summary: ALK-negative Anaplastic Large Cell Lymphoma; Peripherial T Cell Lymphoma,Not Otherwise Specified; Angioimmunoblastic T Cell Lymphoma; Enteropathy Associated T Cell Lymphoma; Hepatosplenic T Cell Lymphoma; Subcutaneous Panniculitis Like T Cell Lymphoma

 

Last Updated: 24 Nov 2013

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Salvia Hispanica Seed in Reducing Risk of Disease Recurrence in Patients With Non-Hodgkin Lymphoma
 

Status: Recruiting

Condition Summary: Adult Nasal Type Extranodal NK/T-Cell Lymphoma; Adult T-Cell Leukemia/Lymphoma; Anaplastic Large Cell Lymphoma; Angioimmunoblastic T-Cell Lymphoma; B Lymphoblastic Leukemia/Lymphoma; Blastic Plasmacytoid Dendritic Cell Neoplasm; Burkitt Leukemia; Central Nervous System Lymphoma; Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma; Diffuse Large B-Cell Lymphoma; Enteropathy-Associated T-Cell Lymphoma; Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue; Grade 1 Follicular Lymphoma; Grade 2 Follicular Lymphoma; Grade 3 Follicular Lymphoma; Hepatosplenic T-Cell Lymphoma; Hodgkin Lymphoma; Lymphoplasmacytic Lymphoma; Mantle Cell Lymphoma; Mediastinal (Thymic) Large B-Cell Lymphoma; Mycosis Fungoides; Nasal Type Extranodal NK/T-Cell Lymphoma; Nodal Marginal Zone Lymphoma; Peripheral T-Cell Lymphoma, Not Otherwise Specified; Post-Transplant Lymphoproliferative Disorder; Primary Cutaneous Anaplastic Large Cell Lymphoma; Primary Effusion Lymphoma; Sezary Syndrome; Splenic Marginal Zone Lymphoma; Subcutaneous Panniculitis-Like T-Cell Lymphoma; Systemic Anaplastic Large Cell Lymphoma; T Lymphoblastic Leukemia/Lymphoma; Transformed Recurrent Non-Hodgkin Lymphoma

 

Last Updated: 28 Jan 2016

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CEOP/IVE/GDP Compared With CEOP as the First-line Therapy for Newly Diagnosed Adult Patients With PTCL
 

Status: Not yet recruiting

Condition Summary: Peripheral T-Cell Lymphoma; Angioimmunoblastic T Cell Lymphoma; ALK-negative Anaplastic Large Cell Lymphoma; Enteropathy Associated T Cell Lymphoma; Subcutaneous Panniculitis Like T Cell Lymphoma; Acute Adult T-Cell Leukemia/Lymphoma

 

Last Updated: 14 Oct 2015

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