Last Modified: November 1, 2001
Table of Contents
CancerMail from the National Cancer Institute
1
UI - 21360537
AU - Linnavuori K; Vaheri A
TI - [Kaposi's sarcoma another new infectious disease?]
SO - Duodecim 1997;113(9):795, 797-8
AD - Department of Virology, Haartman Institute, Helsinki University,
Helsinki, Finland.
2
UI - 21341627
AU - Keller R; Zago A; Viana MC; Bourboulia D; Desgranges C; Casseb J; Moura
WV; Dietze R; Collandre H
TI - HHV-8 infection in patients with AIDS-related Kaposi's sarcoma in
Brazil.
SO - Braz J Med Biol Res 2001 Jul;34(7):879-86
AD - Nucleo de Doencas Infecciosas, Universidade Federal do Espirito Santo,
Vitoria, ES, Brasil. kellygtr@npd.ufes.br
The aims of the present study were to determine the prevalence of human
herpesvirus type 8 (HHV-8) in HIV-positive Brazilian patients with
(HIV+/KS+) and without Kaposi's sarcoma (HIV+/KS-) using PCR and
immunofluorescence assays, to assess its association with KS disease, to
evaluate the performance of these tests in detecting HHV-8 infection,
and to investigate the association between anti-HHV-8 antibody titers,
CD4 counts and staging of KS disease. Blood samples from 66 patients, 39
HIV+/KS+ and 27 HIV+/KS-, were analyzed for HHV-8 viremia in peripheral
blood mononuclear cells by PCR and HHV-8 antigenemia for latent and
lytic infection by immunofluorescence assay. Positive samples for latent
nuclear HHV-8 antigen (LNA) antibodies were titrated out from 1/100 to
(1/4)09,600 dilution. Clinical information was collected from medical
records and risk behavior was assessed through an interview. HHV-8 DNA
sequences were detected by PCR in 74.3% of KS+ patients and in 3.7% of
KS- patients. Serological assays were similar in detecting anti-LNA
antibodies and anti-lytic antigens in sera from KS+ patients (79.5%) and
KS- patients (18.5%). HHV-8 was associated with KS whatever the method
used, i.e., PCR (odds ratio (OR) = 7.4, 95% confidence interval (CI) =
2.16-25.61) or anti-LNA and anti-lytic antibodies (OR = 17.0, 95%CI =
4.91-59.14). Among KS+ patients, HHV-8 titration levels correlated
positively with CD4 counts (rho 0.48, P = 0.02), but not with KS
staging. HHV-8 is involved in the development of KS in different
geographic areas worldwide, as it is in Brazil, where HHV-8 is more
frequent among HIV+ patients. KS severity was associated with
immunodeficiency, but no correlation was found between HHV-8 antibody
titers and KS staging.
3
UI - 21384835
AU - Basilio-de-Oliveira C; Eyer-Silva WA; Valle HA; Rodrigues AL; Pinheiro
Pimentel AL; Morais-De-Sa CA
TI - Mycobacterial spindle cell pseudotumor of the appendix vermiformis in a
patient with aids.
SO - Braz J Infect Dis 2001 Apr;5(2):98-100
AD - Departments of Pathology and Clinical Immunology, Gaffre e Guinle
University Hospital, Rio de Janeiro, RJ, Brazil.
Mycobacterial pseudotumor (MP) is a rare pathologic presentation of both
Mycobacterium tuberculosis and non-tuberculous mycobacterial disease,
hitherto reported to occur only in immunosuppressed patients with or
without human immunodeficiency virus infection. This lesion shares close
pathologic resemblance to certain mesenchymal neoplasms, particularly
Kaposi's sarcoma (KS), from which it must be properly differentiated due
to distinct prognosis and therapy. We report a case of MP obliterating
the lumen of the appendix vermiformis in a 34-year-old patient who died
of complications of AIDS at our hospital in Rio de Janeiro. A total of
24 cases of MP (including our patient) have been described in the
literature. MP has been found especially in lymph nodes, but extranodal
lesions have been described in the skin, spleen, lung, bone marrow,
brain and, in our patient, the appendix vermiformis. We offer a review
of the other 23 published case reports of MP in both HIV-infected and
uninfected patients and discuss the pathologic features that
differentiate MP from KS.
4
UI - 20298916
AU - Jacobson LP; Jenkins FJ; Springer G; Munoz A; Shah KV; Phair J; Zhang Z;
Armenian H
TI - Interaction of human immunodeficiency virus type 1 and human herpesvirus
type 8 infections on the incidence of Kaposi's sarcoma.
SO - J Infect Dis 2000 Jun;181(6):1940-9
AD - Department of Epidemiology, Johns Hopkins University School of Hygiene
and Public Health, Baltimore, MD 21205, USA. ljacobso@jhsph.edu
To determine Kaposi's sarcoma (KS) risk related to timing of human
immunodeficiency virus type 1 (HIV-1) and human herpesvirus type 8
(HHV-8) infections, stored longitudinal sera from 400 homosexual men
with known dates of HIV-1 seroconversion (+/-4.5 months) were tested for
HHV-8 antibody. Times from HHV-8 seroconversion to KS were compared for
the 69 men who became infected with HHV-8 after acquiring HIV-1 to the
182 men who were HHV-8 seropositive before their HIV-1 infection. None
developed KS before coinfection. HHV-8 seroconversion after HIV-1
infection increased the risk of KS (risk ratio, 2.55; 95% confidence
interval, 1.06-6.10) compared with those infected with HHV-8 before
HIV-1. The KS hazards in HHV-8-infected men increased by 60% (P<.001)
for each year of HIV-1 infection. Faster CD4 cell loss and higher HIV-1
RNA levels significantly predicted KS. The quicker development of KS in
men acquiring HHV-8 after HIV-1 and its association with CD4 slope
argues that KS is more likely if HHV-8 infection occurs in an
immunocompromised person.
5
UI - 21162877
AU - Cannon MJ; Pellett PE
TI - Effect of order of infection with human immunodeficiency virus and human
herpesvirus 8 on the incidence of Kaposi's sarcoma.
SO - J Infect Dis 2001 Apr 15;183(8):1304-5
6
UI - 21416872
AU - Alkhuja S; Menkel R; Patel B; Ibrahimbacha A
TI - Stridor and difficult airway in an AIDS patient.
SO - AIDS Patient Care STDS 2001 Jun;15(6):293-5
AD - Division of of Critical Care Medicine, Department of Medicine, St.
Barnabas Hospital, Weill Medical College of Cornell University, Bronx,
New York 10457-2594, USA. salkuja@aol.com
Kaposi's sarcoma (KS) is the most common malignancy observed in patients
with acquired immune deficiency syndrome (AIDS). Although KS involves
the head and neck in AIDS patients, difficult airway due to KS in an
AIDS patient has rarely been reported in the literature. We report a
patient with AIDS and cutaneous KS who developed inspiratory stridor and
required an emergent tracheostomy. AIDS patients with cutaneous KS
should have an assessment of the upper airway even in the absence of
airway-related symptoms. If KS is present in the upper airway, fiber
optic and/or radiologic studies are indicated to assess the extent of
KS, and to define the appropriate interventions.
7
UI - 21352930
AU - Gonzalez-Castillo J; Blanco F; Soriano V; Barreiro P; Concepcion Bravo
M; Jimenez-Nacher I; Gonzalez-Lahoz J
TI - [Opportunistic episodes in patients infected with the human
immunodeficiency virus during the first 6 months of HAART]
SO - Med Clin (Barc) 2001 Jun 23;117(3):81-4
AD - Servicio de Enfermedades Infecciosas, Hospital Carlos III, Instituto de
Salud Carlos III, Madrid. jgdelcastillo@terra.es
BACKGROUND: We aimed at analysing the incidence and characteristics of
opportunistic events (OE) within a few months after starting highly
active antiretroviral therapy (HAART) in HIV infected patients. PATIENTS
AND METHOD: Retrospective study of HIV infected outclinic patients
attended in a HIV/AIDS reference hospital in Madrid, who initiated HAART
during the second semester of 1998, with a baseline CD4 cell count 250 x
10(6) cells/l. We recorded the incidence of OE within 6 months after
beginning HAART and analysed virological and immunological parameters,
sociodemographic variables and types of antiretroviral treatment.
RESULTS: The study included 269 patients. Twenty-one (7.8%) OE were
recorded. At the onset of HAART, the mean CD4 cell count in these 21
patients was 137 (92) x 10(6)/land the median viral load was 24,043
cop/ml. At the time of OE diagnosis, these parameters were 218 (114) x
10(6)/l (p = 0.012) and < 500 cop/ml, respectively. OE were distributed
as follows: herpes zoster, 9 cases (43%), Pneumocystis carinii
pneumonia, 5 cases (24%), Kaposi sarcoma,3 cases (14%) and tuberculosis,
cerebral toxoplasmosis, cytomegalovirus retinitis, and non-Hodgkin
lymphoma, 1 case each. Overall, 78% of OE occurred within first 4 months
after beginning HAART. In addition, an OE was developed by 8% patients
treated with NRTI and PI, 2% treated with NRTI and NNRTI, and 10%
treated with NRTI,NNRTI and PI (p = 0.44). CONCLUSIONS: HIV-infected
subjects with low CD4 counts are prone to develop OE within the first
few moths after beginning HAART. An inflammatory response to latent
antigens due to the immune recovery might explain this fact.
8
UI - 21371954
AU - Aboulafia DM
TI - Kaposi's sarcoma.
SO - Clin Dermatol 2001 May-Jun;19(3):269-83
AD - Division of Hematology/Oncology, Virginia Mason Clinic, Seattle,
Washington 98111, USA. hemdma@vmmc.org