2016
DOI: 10.12890/2016_000493
|View full text |Cite
|
Sign up to set email alerts
|

Kaposi’s Sarcoma Presenting as Lymphadenopathy in an Immunocompetent Patient

Abstract: Introduction Kaposi’s sarcoma (KS) is an angioproliferative disorder first described in 1872 by Moritz Kaposi. Four main clinical presentations of KS have been described: classic, endemic, iatrogenic and epidemic. KS involvement of the lymph nodes is extremely uncommon in the classical variant form, especially if it precedes the skin manifestations. We describe the case of an elderly HIV-negative patient presenting with lymphadenopathy who was found to have KS. Case Report … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
2
1

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 8 publications
0
2
0
Order By: Relevance
“…The involvement of lymph nodes by Kaposi sarcoma is not an uncommon event, accounting for up to 33% of patients with Kaposi sarcoma [16]. The epidemic and endemic forms are the most common forms to show lymph node involvement, while rare cases have been reported in the other forms [17]. It is unclear if isolated Kaposi sarcoma lesions involving lymph nodes represent a primary lymph node disease or a disseminated disease of an involuted cutaneous or visceral primary.…”
Section: Discussionmentioning
confidence: 99%
“…The involvement of lymph nodes by Kaposi sarcoma is not an uncommon event, accounting for up to 33% of patients with Kaposi sarcoma [16]. The epidemic and endemic forms are the most common forms to show lymph node involvement, while rare cases have been reported in the other forms [17]. It is unclear if isolated Kaposi sarcoma lesions involving lymph nodes represent a primary lymph node disease or a disseminated disease of an involuted cutaneous or visceral primary.…”
Section: Discussionmentioning
confidence: 99%
“…The other results included 3 patients with HHV-8-related hemophagocytic syndrome (HS), but no evidence of KS, in a 61-year-old Taiwanese immunocompetent man [ 10 ] and two Italians over sixty years old following steroidal treatment for autoimmune hemolytic anemia [ 11 ]. A localized cutaneous KS, started as inguinal lymph node involvement, was reported in a 67-year-old Tunisian hypertensive and diabetic man [ 12 ]. 8 cases of cutaneous and/or mucosal KS in immunocompetent individuals were also reported (a 77-year-old Irish man, 2 men under 50 years old of unknown origin, a 55-year-old Afro-American man, 4 Turkish men of whom 3 over 70 years old and 1 of 27 years old) [ 13 16 ].…”
Section: Discussionmentioning
confidence: 99%