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1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Hematoxylin-eosin staining revealed the presence of lymphoid cell proliferation&#44; consisting mainly of plasma cells in different stages of maturation&#44; with involvement of striated muscle tissue &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41; and deposition of amorphous&#44; homogeneous&#44; eosinophilic&#44; Congo red&#8211;positive material compatible with amyloid fibrils&#46; Immunohistochemistry revealed &#954; light chain restriction but was negative for &#955; light chain and for CD20 &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a> A and B&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">The staging workup included laboratory tests &#40;complete blood count&#44; biochemistry&#44; &#946;2-microglobulin&#44; and protein electrophoresis&#41;&#44; myelogram&#44; bone marrow biopsy&#44; 24-hour urinary light chain excretion&#44; bone marrow blood count&#44; and bone marrow flow cytometry&#46; The results of all studies were normal&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Primary cutaneous plasmacytoma&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesion was excised and the patient is attending periodic check-ups with no recurrence&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Malignant plasma cell tumors are usually systemic &#40;multiple myeloma&#41; and less often localized &#40;solitary plasmacytoma&#41;&#46; Localized tumors include solitary plasmacytomas of bone and extramedullary plasmacytomas&#46; In 60&#37; to 80&#37; of cases extramedullary plasmacytomas are located in the upper respiratory tract&#46; Primary skin lesions are very rare&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Primary cutaneous plasmacytoma is included in the 2005 classification of the European Organization for Research and Treatment of Cancer &#40;EORTC&#41; among the marginal zone B-cell lymphomas&#44;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> and originates from the clonal proliferation of immunoglobulin-secreting plasma cells in the absence of underlying multiple myeloma&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;3&#8211;5</span></a> It was first described by Stout and Frerichs in 1949<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> and accounts for 4&#37; 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and infectious diseases with significant infiltration of plasma cells&#44; such as syphilis and Lyme disease&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Solitary plasmacytoma progresses to multiple myeloma in one third of cases<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> and cases with multiple or large lesions have the worst prognosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The treatment for solitary tumors is surgery&#44; which may be combined with radiation therapy and intralesional corticosteroid therapy&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;4</span></a><span class="elsevierStyleSup">&#46;</span><a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Chemotherapy should be considered when multiple lesions are present&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflicts of Interest</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case for Diagnosis
Slow-Growing Nodule on the Lower Lip
Nódulo de crecimiento progresivo localizado en el labio inferior
C. Prada-García
Autor para correspondencia
caminoprada@gmail.com

Corresponding author.
, M. Lamoca-Martín, M.Á. Rodríguez-Prieto
Servicio de Dermatología, Complejo Asistencial Universitario de León, León, Spain
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1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Hematoxylin-eosin staining revealed the presence of lymphoid cell proliferation&#44; consisting mainly of plasma cells in different stages of maturation&#44; with involvement of striated muscle tissue &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41; and deposition of amorphous&#44; homogeneous&#44; eosinophilic&#44; Congo red&#8211;positive material compatible with amyloid fibrils&#46; Immunohistochemistry revealed &#954; light chain restriction but was negative for &#955; light chain and for CD20 &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a> A and B&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">The staging workup included laboratory tests &#40;complete blood count&#44; biochemistry&#44; &#946;2-microglobulin&#44; and protein electrophoresis&#41;&#44; myelogram&#44; bone marrow biopsy&#44; 24-hour urinary light chain excretion&#44; bone marrow blood count&#44; and bone marrow flow cytometry&#46; The results of all studies were normal&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Primary cutaneous plasmacytoma&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesion was excised and the patient is attending periodic check-ups with no recurrence&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Malignant plasma cell tumors are usually systemic &#40;multiple myeloma&#41; and less often localized &#40;solitary plasmacytoma&#41;&#46; Localized tumors include solitary plasmacytomas of bone and extramedullary plasmacytomas&#46; In 60&#37; to 80&#37; of cases extramedullary plasmacytomas are located in the upper respiratory tract&#46; Primary skin lesions are very rare&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Primary cutaneous plasmacytoma is included in the 2005 classification of the European Organization for Research and Treatment of Cancer &#40;EORTC&#41; among the marginal zone B-cell lymphomas&#44;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> and originates from the clonal proliferation of immunoglobulin-secreting plasma cells in the absence of underlying multiple myeloma&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;3&#8211;5</span></a> It was first described by Stout and Frerichs in 1949<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> and accounts for 4&#37; of extramedullary plasmacytomas&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">Mean age at diagnosis is 60 years&#44; with a male-female ratio of 4&#58;1&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;4&#44;6</span></a> Clinically it presents as a slow-growing papule&#44; plaque&#44; or erythematous-violaceous nodule<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;5</span></a> usually located on the trunk or in the facial region&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> It can take the form of a solitary tumor &#40;62&#37;&#41; or may involve multiple sites &#40;38&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Histopathology shows a nonepidermotropic dermal infiltrate of plasma cells at different stages of maturation&#46; Immunohistochemistry is usually positive for CD79a&#44; CD38&#44; and CD138 and negative for CD20 and leukocyte common antigen&#59; monotypic expression of immunoglobulin light chains is common&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> Since amyloid deposits are more often associated with secondary plasmacytomas&#44; their presence should raise suspicion of an extracutaneous origin&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a> Diagnosis is based on clinical&#44; histopathologic&#44; and immunohistochemical findings&#44; and multiple myeloma must be ruled out by laboratory&#44; radiologic&#44; and bone marrow studies&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Differential diagnosis is mainly with secondary cutaneous plasmacytoma&#44; mucosal extramedullary plasmacytoma with secondary skin involvement&#44; other primary B-cell lymphomas&#44; and infectious diseases with significant infiltration of plasma cells&#44; such as syphilis and Lyme disease&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Solitary plasmacytoma progresses to multiple myeloma in one third of cases<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> and cases with multiple or large lesions have the worst prognosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The treatment for solitary tumors is surgery&#44; which may be combined with radiation therapy and intralesional corticosteroid therapy&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;4</span></a><span class="elsevierStyleSup">&#46;</span><a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Chemotherapy should be considered when multiple lesions are present&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflicts of Interest</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Información del artículo
ISSN: 15782190
Idioma original: Inglés
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2019 Octubre 0 3 3
2019 Septiembre 4 2 6
2019 Agosto 4 3 7
2019 Julio 4 5 9
2019 Junio 4 18 22
2019 Mayo 4 10 14
2019 Abril 2 13 15
2019 Marzo 0 7 7
2019 Febrero 2 2 4
2019 Enero 2 2 4
2018 Diciembre 2 5 7
2018 Noviembre 3 2 5
2018 Octubre 3 0 3
2018 Septiembre 1 0 1
2018 Mayo 0 1 1
2018 Marzo 0 1 1
2018 Febrero 74 3 77
2018 Enero 74 9 83
2017 Diciembre 101 6 107
2017 Noviembre 59 8 67
2017 Octubre 64 6 70
2017 Septiembre 73 5 78
2017 Agosto 62 14 76
2017 Julio 57 13 70
2017 Junio 73 36 109
2017 Mayo 68 10 78
2017 Abril 59 11 70
2017 Marzo 55 21 76
2017 Febrero 55 11 66
2017 Enero 55 6 61
2016 Diciembre 71 9 80
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2016 Octubre 73 20 93
2016 Septiembre 66 14 80
2016 Agosto 89 23 112
2016 Julio 75 20 95
2016 Junio 7 18 25
2016 Mayo 7 8 15
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2015 Agosto 13 7 20
2015 Julio 87 8 95
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2015 Mayo 112 12 124
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2013 Diciembre 35 7 42
2013 Noviembre 26 5 31
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2013 Julio 16 11 27
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2013 Mayo 9 7 16
2013 Abril 15 8 23
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2013 Febrero 21 4 25
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2012 Diciembre 24 4 28
2012 Agosto 0 1 1
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