scholarly journals Involution of classic Kaposi sarcoma lesions under acitretin treatment Kaposi sarcoma treated with acitretin

2020 ◽  
Vol 8 (12) ◽  
pp. 3340-3343
Author(s):  
Najla Daadaa ◽  
Asmahane Souissi ◽  
Meryam Chaabani ◽  
Ines Chelly ◽  
Moez Ben Salem ◽  
...  
Keyword(s):  
Kaposi Sarcoma ◽  
Classic Kaposi Sarcoma

scholarly journals Risk of Classic Kaposi Sarcoma with Residential Exposure to Volcanic and Related Soils in Sicily

2009 ◽  
Vol 19 (8) ◽  
pp. 597-601 ◽  
Author(s):  
Colleen Pelser ◽  
Carmelo Dazzi ◽  
Barry I. Graubard ◽  
Carmela Lauria ◽  
Francesco Vitale ◽  
...  
Keyword(s):  
Kaposi Sarcoma ◽  
Residential Exposure ◽  
Classic Kaposi Sarcoma

Disseminated classic Kaposi sarcoma in a seven-year-old girl

2021 ◽  
Vol 31 (2) ◽  
pp. 269-270
Author(s):  
Thilo Gambichler ◽  
Victoria Brown ◽  
Alicia Siebold ◽  
Markus Stücker ◽  
Maria Bakirtzi
Keyword(s):  
Kaposi Sarcoma ◽  
Classic Kaposi Sarcoma

Familial Classic Kaposi Sarcoma in Two Siblings: Case Report and Literature Review

2013 ◽  
Vol 17 (5) ◽  
pp. 356-361 ◽  
Author(s):  
Mohammad Almohideb ◽  
A. Kevin Waiters ◽  
William Gerstein
Keyword(s):  
Laboratory Data ◽  
Kaposi Sarcoma ◽  
Immune Deficiency Syndrome ◽  
Deficiency Syndrome ◽  
Eastern European ◽  
Familial Cases ◽  
Vascular Proliferation ◽  
Classic Kaposi Sarcoma ◽  
Acquired Immune Deficiency

Background: Kaposi sarcoma (KS) is a cutaneous endothelial vascular proliferation with four subtypes: iatrogenic, acquired immune deficiency syndrome (AIDS) related, African, and classic. Familial cases of KS are rare, with 72 cases reported to date, and all were described with the classic variant. The occurrence of classic KS in the Jewish population is well documented, and most of the familial classic KS cases were also reported in Jewish families. Objective: We briefly present the history, biopsies, laboratory data, diagnosis, and treatment of localized lower limb classic KS in two siblings of Jewish Eastern European ethnic descent with their response to different therapy modalities. One of our cases had the second longest reported period of follow-up for familial classic KS of 40 years.

scholarly journals Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome Sequencing

2019 ◽  
Vol 6 (10) ◽  
Author(s):  
Sanni J Rinne ◽  
Lauri J Sipilä ◽  
Päivi Sulo ◽  
Emmanuelle Jouanguy ◽  
Vivien Béziat ◽  
...  
Keyword(s):  
Whole Genome Sequencing ◽  
Genome Sequencing ◽  
Kaposi Sarcoma ◽  
The Other ◽  
Whole Genome ◽  
Genome Wide ◽  
Starting Point ◽  
Familial Clustering ◽  
Iranian Family ◽  
Classic Kaposi Sarcoma

Abstract Familial clustering of classic Kaposi sarcoma (CKS) is rare with, approximately 100 families reported to date. We studied 2 consanguineous families, 1 Iranian and 1 Israeli, with multiple cases of adult CKS and without overt underlying immunodeficiency. We performed genome-wide linkage analysis and whole-genome sequencing to discover the putative genetic cause for predisposition. A 9-kb homozygous intronic deletion in RP11-259O2.1 in the Iranian family and 2 homozygous variants, 1 in SCUBE2 and the other in CDHR5, in the Israeli family were identified as possible candidates. The presented variants provide a robust starting point for validation in independent samples.

scholarly journals Isolated classic Kaposi Sarcoma in an old female patient

2014 ◽  
Vol 4 (2) ◽  
Author(s):  
Nursel Dilek ◽  
Aziz Ramazan Dilek ◽  
Yunus Saral ◽  
Recep Bedir
Keyword(s):  
Female Patient ◽  
Kaposi Sarcoma ◽  
Classic Kaposi Sarcoma
Sign in / Sign up

Export Citation Format

Share Document