Ca. Pelaez et al., MOLLUSCUM CONTAGIOSUM, INVOLVING THE UPPER EYELIDS, IN A CHILD INFECTED WITH HIV-1, Pediatric AIDS and HIV infection, 7(1), 1996, pp. 43-46
Background. Infection with molluscum contagiosum has been reported in
pediatric and adult patients with acquired immune deficiency syndrome
(AIDS), but rarely affecting eyelids. We have studied the viral phenot
ype, HIV-1 plasma viremia, p24 antigenemia, alterations of cellular im
mune function, and the ophthalmological status in a 5-year old human i
mmunodeficiency virus type 1 infected girl, who developed multiple mol
luscum lesions, bilaterally involving upper eyelids with extension ove
r the face and nose. Methods. Detailed ophthalmological examination an
d immunological and virological studies were performed in a pediatric
patient with HIV-1 vertical infection having extensive infection with
molluscum contagiosum. Results. The pediatric patient was emetropic; t
ricomegalia was present bilaterally, and alteration of the microvessel
s of the conjunctiva (microangiopathy) was observable in both eyes and
structural (fibrilar) degeneration of the vitreous architecture in bo
th eyes. There was no ophthalmoscopic sign of infectious retinitis or
retinal microangiopathy. She had lymphopenia, very low percentage and
absolute number of CD4(+) T cells but increased percentage of CD8(+) T
cells. The in vitro lymphocyte proliferative response to phytohemaglu
ttinin (PHA) was depressed as compared to healthy controls. She had hi
gh levels of viral HIV RNA in her plasma and of p24 antigen in her ser
um, and the phenotype of the isolated HIV-1 was determined to be syncy
tium-inducing (SI). Conclusion. Although healthy persons may develop m
olluscum contagiosum, usually unilateral, as far as we are aware this
report is the first to document a case of molluscum contagiosum with b
ilateral eyelid involvement in an HIV-1-infected pediatric patient. Ou
r observations suggest that this type of infection may be present in H
IV-infected children, associated with high viral load and possibly an
SI viral phenotype, severe immunoregulatory abnormalities, and poor cl
inical status.