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reduced absolute CD4 lymphocyte count &#40;197&#47;&#956;L&#41;&#44; increased absolute CD8 lymphocyte count &#40;1291&#47;&#956;L&#41;&#44; and a low viral load &#40;1293&#47;mL&#41;&#46; Computed tomography of the chest revealed centrilobular emphysema but no masses or enlarged nodes&#46; Abdominal ultrasound revealed a hypertrophic prostate with an adenomatous appearance&#46; The electrocardiogram revealed mild tricuspid insufficiency&#46; No findings of interest were observed in the computed tomography of the head&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">These data confirmed a diagnosis of HIV-associated atypical cutaneous CD8<span class="elsevierStyleSup">&#43;</span> T-cell infiltrate or cutaneous CD8<span class="elsevierStyleSup">&#43;</span> pseudolymphoma&#46; After 3 months of systemic antiretroviral therapy &#40;ritonavir&#44; atazanavir&#44; emtricitabine&#44; and tenofovir&#41; and tapered oral prednisolone &#40;starting at 45<span class="elsevierStyleHsp" style=""></span>mg&#47;d&#41;&#44; the patient&#39;s progress was good&#44; with a decrease in the number of lesions&#44; resolution of pruritus&#44; and weight gain&#46; In addition&#44; the hair on his scalp and eyebrows began to grow back again &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0035" class="elsevierStylePara elsevierViewall">Mucocutaneous disorders are very common in HIV-infected patients&#46; Lymphomas are the second most common HIV-associated malignancy after Kaposi sarcoma&#46; Most cases involve non-Hodgkin lymphoma&#44; with a higher incidence of aggressive B-cell subtypes and extranodal disease&#44;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a> although cases of cutaneous T-cell lymphoma have also been reported&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;3</span></a> HIV-associated polyclonal lymphoproliferative disorders have recently been reported<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;4&#44;5</span></a>&#59; however&#44; these can mimic cutaneous T-cell lymphoma both clinically and histologically&#44; as occurred in the case we report&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;7</span></a> Cutaneous CD8<span class="elsevierStyleSup">&#43;</span> pseudolymphoma is uncommon in HIV-infected patients and its pathogenesis poorly understood&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;6</span></a> It usually presents as extensive plaques or erythroderma<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2&#44;4&#44;6&#44;8</span></a> and is often associated with eosinophilia&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Histology generally reveals a massive dermal infiltrate composed of CD8<span class="elsevierStyleSup">&#43;</span> T cells&#44; with or without involvement of the epidermis&#44; and negative results in the clonality study&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#8211;4&#44;6</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The literature contains few cases of HIV-associated cutaneous CD8<span class="elsevierStyleSup">&#43;</span> pseudolymphoma&#44;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;4&#44;6&#44;7</span></a> which usually appears in later stages of the disease and is associated with severe CD4 lymphopenia&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2&#44;6</span></a> The disease is usually treated with systemic corticosteroids&#44; although a favorable response to antiretroviral therapy has been reported&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">In our patient&#44; diagnosis was based on the correlation between clinical and pathology findings&#44; including clinical course&#44; response to antiretroviral therapy&#44; and the results of immunohistochemistry and the molecular biology techniques used for the clonality study&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">In conclusion&#44; this diagnosis should be considered when an HIV-infected patient has intensely pruritic skin infiltration&#44; alopecia universalis&#44; weight loss&#44; and eosinophilia&#46; Nevertheless&#44; differential diagnosis should include cutaneous T-cell lymphoma&#44; primary hypereosinophilic syndrome &#40;&#62;1500&#47;&#956;L in peripheral blood for more than 6 months with no other apparent explanation&#41;&#44; toxicoderma&#44; atopic dermatitis&#44; contact dermatitis&#44; parasitic infestation&#44; and other HIV-associated skin diseases&#44; such as papuloerythroderma of Ofuji&#46;</p></span>"
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Cases and Research Letters
Cutaneous CD8+ T-cell Infiltrates Associated With Human Immunodeficiency Virus
Infiltración cutánea por linfocitos T CD8+ asociada a virus de la inmunodeficiencia humana
T. Fernández-Moranoa,
Autor para correspondencia
tfm_84@hotmail.com

Corresponding author.
, M. Aguilar-Berniera, J. del Boza, R. Fúnez-Liébanab
a Servicio de Dermatología, Hospital Costa del Sol, Marbella, Spain
b Servicio de Anatomía Patológica, Hospital Costa del Sol, Marbella, Spain
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Staining for CD30 was negative &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Testing to detect clonal rearrangement of the immunoglobulin heavy chain gene &#40;JH segment&#41; and T-&#947; and T-&#946; receptor gene was negative&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">The patient was admitted for evaluation of a constitutional syndrome&#46; The most notable findings in the laboratory workup were elevated peripheral eosinophil counts and frequency &#40;570&#47;&#956;L&#44; 20&#46;9&#37;&#41; and a high lactate dehydrogenase concentration &#40;877 U&#47;L&#41;&#46; Serology for HIV was positive&#44; whereas tests for other entities &#40;syphilis&#44; hepatitis B virus&#44; hepatitis C virus&#44; cytomegalovirus&#44; and Epstein-Barr virus&#41; and tumor markers were negative&#46; Cytometry revealed a low CD4&#58;CD8 ratio &#40;0&#46;15&#59; reference range&#44; 1-4&#41;&#44; reduced absolute CD4 lymphocyte count &#40;197&#47;&#956;L&#41;&#44; increased absolute CD8 lymphocyte count &#40;1291&#47;&#956;L&#41;&#44; and a low viral load &#40;1293&#47;mL&#41;&#46; Computed tomography of the chest revealed centrilobular emphysema but no masses or enlarged nodes&#46; Abdominal ultrasound revealed a hypertrophic prostate with an adenomatous appearance&#46; The electrocardiogram revealed mild tricuspid insufficiency&#46; No findings of interest were observed in the computed tomography of the head&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">These data confirmed a diagnosis of HIV-associated atypical cutaneous CD8<span class="elsevierStyleSup">&#43;</span> T-cell infiltrate or cutaneous CD8<span class="elsevierStyleSup">&#43;</span> pseudolymphoma&#46; After 3 months of systemic antiretroviral therapy &#40;ritonavir&#44; atazanavir&#44; emtricitabine&#44; and tenofovir&#41; and tapered oral prednisolone &#40;starting at 45<span class="elsevierStyleHsp" style=""></span>mg&#47;d&#41;&#44; the patient&#39;s progress was good&#44; with a decrease in the number of lesions&#44; resolution of pruritus&#44; and weight gain&#46; In addition&#44; the hair on his scalp and eyebrows began to grow back again &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0035" class="elsevierStylePara elsevierViewall">Mucocutaneous disorders are very common in HIV-infected patients&#46; Lymphomas are the second most common HIV-associated malignancy after Kaposi sarcoma&#46; Most cases involve non-Hodgkin lymphoma&#44; with a higher incidence of aggressive B-cell subtypes and extranodal disease&#44;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a> although cases of cutaneous T-cell lymphoma have also been reported&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;3</span></a> HIV-associated polyclonal lymphoproliferative disorders have recently been reported<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;4&#44;5</span></a>&#59; however&#44; these can mimic cutaneous T-cell lymphoma both clinically and histologically&#44; as occurred in the case we report&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;7</span></a> Cutaneous CD8<span class="elsevierStyleSup">&#43;</span> pseudolymphoma is uncommon in HIV-infected patients and its pathogenesis poorly understood&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;6</span></a> It usually presents as extensive plaques or erythroderma<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2&#44;4&#44;6&#44;8</span></a> and is often associated with eosinophilia&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Histology generally reveals a massive dermal infiltrate composed of CD8<span class="elsevierStyleSup">&#43;</span> T cells&#44; with or without involvement of the epidermis&#44; and negative results in the clonality study&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#8211;4&#44;6</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The literature contains few cases of HIV-associated cutaneous CD8<span class="elsevierStyleSup">&#43;</span> pseudolymphoma&#44;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;4&#44;6&#44;7</span></a> which usually appears in later stages of the disease and is associated with severe CD4 lymphopenia&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2&#44;6</span></a> The disease is usually treated with systemic corticosteroids&#44; although a favorable response to antiretroviral therapy has been reported&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">In our patient&#44; diagnosis was based on the correlation between clinical and pathology findings&#44; including clinical course&#44; response to antiretroviral therapy&#44; and the results of immunohistochemistry and the molecular biology techniques used for the clonality study&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">In conclusion&#44; this diagnosis should be considered when an HIV-infected patient has intensely pruritic skin infiltration&#44; alopecia universalis&#44; weight loss&#44; and eosinophilia&#46; Nevertheless&#44; differential diagnosis should include cutaneous T-cell lymphoma&#44; primary hypereosinophilic syndrome &#40;&#62;1500&#47;&#956;L in peripheral blood for more than 6 months with no other apparent explanation&#41;&#44; toxicoderma&#44; atopic dermatitis&#44; contact dermatitis&#44; parasitic infestation&#44; and other HIV-associated skin diseases&#44; such as papuloerythroderma of Ofuji&#46;</p></span>"
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