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nasal type&#59; &#947;&#47;&#948; T-cell lymphoma&#44; angioinvasive &#40;type E&#41; lymphomatoid papulosis&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a> or B-cell lymphoma rich in angioinvasive T cells<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">2</span></a>&#41;&#46; The new immunohistochemistry analysis was positive for CD3&#44; CD5&#44; CD7&#44; and &#946;F1&#44; and showed expression of granzyme B and TIA-1&#46; CD2&#44; CD4&#44; CD8&#44; and CD30 expression was negative&#44; as was CD56&#44; CD20&#44; EBER&#44; and TCR-&#947; expression &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#44; C and D&#41;&#46; Clonality of the <span class="elsevierStyleItalic">TCR-&#947;</span> gene was once again demonstrated on PCR&#44; with a clonal peak of identical size to that of the earlier lesions&#46; The other additional tests&#44; including computed tomography and bone-marrow biopsy were normal&#46; Two months later the patient died as a result of rapidly progressive septicemia&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">In the majority of cases of MF&#44; immunophenotypic expression is CD3<span class="elsevierStyleSup">&#43;</span>&#44; CD4<span class="elsevierStyleSup">&#43;</span> and CD8<span class="elsevierStyleSup">&#8722;</span>&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">3&#44;4</span></a> Some cases show a cytotoxic&#47;suppressor profile &#40;CD3<span class="elsevierStyleSup">&#43;</span>&#44; CD4<span class="elsevierStyleSup">&#8722;</span>&#44; CD8<span class="elsevierStyleSup">&#43;</span>&#41;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">5&#44;6</span></a> or other aberrant phenotypes&#46; Immunophenotypic shift during disease progression is rare&#44; with only 2 cases reported in the literature&#46; In the first of those cases&#44; 5 years after a diagnosis of CD4<span class="elsevierStyleSup">&#43;</span>&#47;CD8<span class="elsevierStyleSup">&#8722;</span> MF with lesions on the trunk&#44; the patient presented cutaneous tumors associated with a loss of vision in the left eye&#46; Histopathology of the globe showed infiltration of the vitreous by atypical CD8<span class="elsevierStyleSup">&#43;</span> lymphocytes&#44; with a CD4&#58;CD8 ratio of 1&#58;4&#46; Although clonal rearrangement of the <span class="elsevierStyleItalic">TCR</span> gene was not mentioned&#44; lesion progression to a tumor phase with concomitant involvement of the vitreous would suggest that the same lymphoproliferative process was the origin&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">7</span></a> In the second case&#44; the diagnosis was also CD4<span class="elsevierStyleSup">&#43;</span>&#47;CD8<span class="elsevierStyleSup">&#8722;</span> MF&#46; After a number of recurrences&#44; the patient developed ulcerated lesions on the lower limbs&#59; the immunohistochemical changes also consisted of a loss of CD4 expression and an increase in the number of CD8<span class="elsevierStyleSup">&#43;</span> atypical lymphocytes&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">8</span></a> Clonal rearrangement of the <span class="elsevierStyleItalic">TCR</span> gene was detected&#44; and comparison of the initial CD4<span class="elsevierStyleSup">&#43;</span> lesions with the later CD8<span class="elsevierStyleSup">&#43;</span> lesions showed the clonal peaks to be of identical size&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">In our patient&#44; neither CD4 nor CD8 expression was detected in the immunophenotypic study of the ulcerated tumor plaque&#44; but the clonal peaks were of an identical size to those in the initial lesions&#59; this therefore indicated that the lesions with distinct clinical and immunophenotypic characteristics were clonally related&#46; To date&#44; there are no reports of cases with loss of CD4 expression&#46; The mechanism that produces the changes in immunophenotype is unknown&#46; This phenomenon is considered common in the case of some childhood B- and T-cell leukemias&#59; however&#44; reports of such changes in the case of B-cell or T-cell lymphoma are rare in the literature&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">We have presented the first case of MF with shift to a double-negative immunophenotype &#40;CD4<span class="elsevierStyleSup">&#8722;</span>&#47;CD8<span class="elsevierStyleSup">&#8722;</span>&#41;&#44; associated with lymphocytes with a greater degree of atypia&#44; pleomorphism&#44; and larger size&#59; these lymphocytes adopted an angiocentric distribution and acquired a cytotoxic profile with TIA-1 expression&#46; Looking at the clinical course both of our case and of the previous cases&#44; we can state that this phenomenon may be associated with disease progression&#44; although more cases are required to be able to draw significant conclusions&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case and Research Letter
Immunophenotypic Shift Associated With Angiocentricity and Cytoxic Characteristics in a Case of Mycosis Fungoides
Cambio de inmunofenotipo asociado a angiocentricidad y características citotóxicas en un caso de micosis fungoide
Á. Vargas Nevadoa,
Autor para correspondencia
avargasn88@gmail.com

Corresponding author.
, N. López Navarroa, E. Gallego Domínguezb, E. Herrera Ceballosa
a Servicio de Dermatología, Hospital Universitario Virgen de la Victoria, Málaga, Spain
b Servicio de Anatomía Patológica, Hospital Universitario Virgen de la Victoria, Málaga, Spain
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showing a tendency to epidermotropism&#44; forming large intraepidermal aggregates &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>B&#41;&#46; Large lymphocytes accounted for less than 25&#37; of the cells of the infiltrate&#46; Immunohistochemistry was positive for CD2&#44; CD3&#44; CD4&#44; CD5&#44; CD6&#44; and CD7&#46; The CD8 antigen was focally positive in the dermis&#44; the CD4&#58;CD8 ratio was 4&#58;1&#44; and CD30 was intensely expressed in the intraepidermal lymphocytes &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#44; C and D&#41;&#46; Polymerase chain reaction analysis detected T-cell receptor &#40;<span class="elsevierStyleItalic">TCR</span>&#41; &#947;-chain gene clonal rearrangement&#46; No expression of CD56&#44; TIA-1&#44; or granzyme B was detected&#46; There were no significant changes on other additional laboratory tests&#46; Based on these findings&#44; we made a diagnosis of MF-type primary cutaneous T-cell lymphoma&#44; stage<span class="elsevierStyleHsp" style=""></span>IB&#46; Treatment was initiated with topical corticosteroids and psoralen&#8211;UV-A&#44; with partial improvement of the skin lesions&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">At 6 months the patient developed a large ulcerating necrotic tumor plaque with erythematous-violaceous borders on the medial surface of the left lower leg &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>A&#41;&#46; Further biopsies were taken and a monomorphic infiltrate of large atypical lymphocytes was seen to affect the full thickness of the dermis with extension into the subcutaneous adipose tissue&#46; There was a notable angiocentricity&#44; with blood vessel necrosis and invasion of vessel walls by the atypical lymphocytes &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>B&#41;&#46; Our differential diagnosis based on these data included progression of MF or the onset and a new lymphoproliferative process &#40;extranodal NK&#47;T-cell lymphoma&#44; nasal type&#59; &#947;&#47;&#948; T-cell lymphoma&#44; angioinvasive &#40;type E&#41; lymphomatoid papulosis&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a> or B-cell lymphoma rich in angioinvasive T cells<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">2</span></a>&#41;&#46; The new immunohistochemistry analysis was positive for CD3&#44; CD5&#44; CD7&#44; and &#946;F1&#44; and showed expression of granzyme B and TIA-1&#46; CD2&#44; CD4&#44; CD8&#44; and CD30 expression was negative&#44; as was CD56&#44; CD20&#44; EBER&#44; and TCR-&#947; expression &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#44; C and D&#41;&#46; Clonality of the <span class="elsevierStyleItalic">TCR-&#947;</span> gene was once again demonstrated on PCR&#44; with a clonal peak of identical size to that of the earlier lesions&#46; The other additional tests&#44; including computed tomography and bone-marrow biopsy were normal&#46; Two months later the patient died as a result of rapidly progressive septicemia&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">In the majority of cases of MF&#44; immunophenotypic expression is CD3<span class="elsevierStyleSup">&#43;</span>&#44; CD4<span class="elsevierStyleSup">&#43;</span> and CD8<span class="elsevierStyleSup">&#8722;</span>&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">3&#44;4</span></a> Some cases show a cytotoxic&#47;suppressor profile &#40;CD3<span class="elsevierStyleSup">&#43;</span>&#44; CD4<span class="elsevierStyleSup">&#8722;</span>&#44; CD8<span class="elsevierStyleSup">&#43;</span>&#41;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">5&#44;6</span></a> or other aberrant phenotypes&#46; Immunophenotypic shift during disease progression is rare&#44; with only 2 cases reported in the literature&#46; In the first of those cases&#44; 5 years after a diagnosis of CD4<span class="elsevierStyleSup">&#43;</span>&#47;CD8<span class="elsevierStyleSup">&#8722;</span> MF with lesions on the trunk&#44; the patient presented cutaneous tumors associated with a loss of vision in the left eye&#46; Histopathology of the globe showed infiltration of the vitreous by atypical CD8<span class="elsevierStyleSup">&#43;</span> lymphocytes&#44; with a CD4&#58;CD8 ratio of 1&#58;4&#46; Although clonal rearrangement of the <span class="elsevierStyleItalic">TCR</span> gene was not mentioned&#44; lesion progression to a tumor phase with concomitant involvement of the vitreous would suggest that the same lymphoproliferative process was the origin&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">7</span></a> In the second case&#44; the diagnosis was also CD4<span class="elsevierStyleSup">&#43;</span>&#47;CD8<span class="elsevierStyleSup">&#8722;</span> MF&#46; After a number of recurrences&#44; the patient developed ulcerated lesions on the lower limbs&#59; the immunohistochemical changes also consisted of a loss of CD4 expression and an increase in the number of CD8<span class="elsevierStyleSup">&#43;</span> atypical lymphocytes&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">8</span></a> Clonal rearrangement of the <span class="elsevierStyleItalic">TCR</span> gene was detected&#44; and comparison of the initial CD4<span class="elsevierStyleSup">&#43;</span> lesions with the later CD8<span class="elsevierStyleSup">&#43;</span> lesions showed the clonal peaks to be of identical size&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">In our patient&#44; neither CD4 nor CD8 expression was detected in the immunophenotypic study of the ulcerated tumor plaque&#44; but the clonal peaks were of an identical size to those in the initial lesions&#59; this therefore indicated that the lesions with distinct clinical and immunophenotypic characteristics were clonally related&#46; To date&#44; there are no reports of cases with loss of CD4 expression&#46; The mechanism that produces the changes in immunophenotype is unknown&#46; This phenomenon is considered common in the case of some childhood B- and T-cell leukemias&#59; however&#44; reports of such changes in the case of B-cell or T-cell lymphoma are rare in the literature&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">We have presented the first case of MF with shift to a double-negative immunophenotype &#40;CD4<span class="elsevierStyleSup">&#8722;</span>&#47;CD8<span class="elsevierStyleSup">&#8722;</span>&#41;&#44; associated with lymphocytes with a greater degree of atypia&#44; pleomorphism&#44; and larger size&#59; these lymphocytes adopted an angiocentric distribution and acquired a cytotoxic profile with TIA-1 expression&#46; Looking at the clinical course both of our case and of the previous cases&#44; we can state that this phenomenon may be associated with disease progression&#44; although more cases are required to be able to draw significant conclusions&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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