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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">The patient was a 90-year-old woman who had a personal history of severe hypoacusis and osteoporosis and was not receiving chronic treatment&#46; She consulted for several asymptomatic lesions on her chest&#44; shoulders&#44; and upper back&#46; The lesions had appeared suddenly 5 years earlier&#44; had never been treated&#44; and had been stable since first onset&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed multiple well-defined erythematous-violaceous telangiectatic macules ranging in diameter from 5<span class="elsevierStyleHsp" style=""></span>mm to 4<span class="elsevierStyleHsp" style=""></span>cm &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The lesions did not blanch with pressure and were negative for the Darier sign&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histologic examination revealed dilated vascular structures in the superficial capillary plexus with peripheral inflammatory infiltrate characterized by a predominance of mast cells &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Staining showed the mast cells to be tryptase-positive &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Telangiectasia macularis eruptiva perstans &#40;TMEP&#41;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0030" class="elsevierStylePara elsevierViewall">The laboratory workup included a complete blood cell count&#44; biochemistry&#44; liver and kidney function tests&#44; and a serum tryptase test&#46; Serum tryptase was slightly elevated at 16&#46;3<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;L &#40;13&#46;5<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;L being the upper limit of normal&#41;&#46; Despite this finding&#44; the patient and her family declined to continue with the exploration due to the patient&#39;s advanced age&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Mastocytosis comprises a group of diseases characterized by an excessive accumulation of mast cells in the skin&#44; and occasionally in the tissue of other organs&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Three clinical variants of mastocytosis with cutaneous involvement have been described&#58; urticaria pigmentosa &#40;either its typical clinical manifestation of plaques and nodules or TMEP&#41;&#44; diffuse cutaneous mastocytosis&#44; and mastocytoma&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">TMEP was first described by Weber in 1930&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Thought to be a rare subtype of urticaria pigmentosa&#44; it occurs in less than 1&#37; of mastocytosis patients&#46; TMEP occurs mainly in young and middle-aged adults&#44; although cases of pediatric onset have been reported&#46; A familial form of TMEP was described in 4 pediatric patients in 3 generations of a single family&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">It manifests clinically as erythematous macules comprising purplish or brownish asymptomatic telangiectasias that are negative for the Darier sign and located primarily on the trunk and upper limbs&#46; Unilateral segmental manifestations of TMEP that may lead to a differential diagnosis with unilateral nevoid telangiectasia have also been reported&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">Histologically&#44; TMEP is characterized by an increase in the relative number of mast cells distributed around dilated capillaries and venules in the superficial capillary plexus&#46; In most cases of TMEP&#44; the number of mast cells does not increase very much in absolute terms&#44; making it difficult to diagnose the disease by means of hematoxylin&#8211;eosin staining&#46; Therefore&#44; immunohistochemical staining for tryptase and&#47;or c-kit &#40;CD 117&#41; is recommended&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Although TMEP has been considered to be a form of mastocytosis that only affects the skin&#44; it can cause systemic symptoms&#44; such as hypotension&#44; flushing&#44; pruritus&#44; abdominal pain&#44; and anaphylaxis due to the release of mediators by mast cells&#46; In other cases&#44; it can lead to symptoms caused by the infiltration of other organs&#44; such as splenomegaly&#44; adenopathy&#44; hepatomegaly&#44; and anemia&#46; Finally&#44; in isolated cases&#44; this variant of mastocytosis has been associated with myeloproliferative&#44; lymphoproliferative&#44; and myelodysplastic syndromes&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">The choice of treatment depends on whether systemic or exclusively cutaneous involvement is detected&#46; Cases involving only the skin have been treated satisfactorily with topical and intralesional corticosteroids&#44; topical calcineurin inhibitors&#44; 585<span class="elsevierStyleHsp" style=""></span>nm vascular laser treatment&#44; and psoralen-UV-A &#40;PUVA&#41; therapy&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflicts of Interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case for Diagnosis
Telangiectatic Macules in a 90-Year-Old Woman
Lesiones maculares telangiectásicas en mujer de 90 años
A. Martín-Fuentes
Corresponding author
adriana.mar.fuen@gmail.com

Corresponding author.
, M.A. Pastor-Nieto, E. De Eusebio-Murillo
Departamento de Dermatología, Hospital Universitario de Guadalajara, Guadalajara, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">The patient was a 90-year-old woman who had a personal history of severe hypoacusis and osteoporosis and was not receiving chronic treatment&#46; She consulted for several asymptomatic lesions on her chest&#44; shoulders&#44; and upper back&#46; The lesions had appeared suddenly 5 years earlier&#44; had never been treated&#44; and had been stable since first onset&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed multiple well-defined erythematous-violaceous telangiectatic macules ranging in diameter from 5<span class="elsevierStyleHsp" style=""></span>mm to 4<span class="elsevierStyleHsp" style=""></span>cm &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The lesions did not blanch with pressure and were negative for the Darier sign&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histologic examination revealed dilated vascular structures in the superficial capillary plexus with peripheral inflammatory infiltrate characterized by a predominance of mast cells &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Staining showed the mast cells to be tryptase-positive &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Telangiectasia macularis eruptiva perstans &#40;TMEP&#41;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0030" class="elsevierStylePara elsevierViewall">The laboratory workup included a complete blood cell count&#44; biochemistry&#44; liver and kidney function tests&#44; and a serum tryptase test&#46; Serum tryptase was slightly elevated at 16&#46;3<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;L &#40;13&#46;5<span class="elsevierStyleHsp" style=""></span>&#956;g&#47;L being the upper limit of normal&#41;&#46; Despite this finding&#44; the patient and her family declined to continue with the exploration due to the patient&#39;s advanced age&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Mastocytosis comprises a group of diseases characterized by an excessive accumulation of mast cells in the skin&#44; and occasionally in the tissue of other organs&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Three clinical variants of mastocytosis with cutaneous involvement have been described&#58; urticaria pigmentosa &#40;either its typical clinical manifestation of plaques and nodules or TMEP&#41;&#44; diffuse cutaneous mastocytosis&#44; and mastocytoma&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">TMEP was first described by Weber in 1930&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Thought to be a rare subtype of urticaria pigmentosa&#44; it occurs in less than 1&#37; of mastocytosis patients&#46; TMEP occurs mainly in young and middle-aged adults&#44; although cases of pediatric onset have been reported&#46; A familial form of TMEP was described in 4 pediatric patients in 3 generations of a single family&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">It manifests clinically as erythematous macules comprising purplish or brownish asymptomatic telangiectasias that are negative for the Darier sign and located primarily on the trunk and upper limbs&#46; Unilateral segmental manifestations of TMEP that may lead to a differential diagnosis with unilateral nevoid telangiectasia have also been reported&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">Histologically&#44; TMEP is characterized by an increase in the relative number of mast cells distributed around dilated capillaries and venules in the superficial capillary plexus&#46; In most cases of TMEP&#44; the number of mast cells does not increase very much in absolute terms&#44; making it difficult to diagnose the disease by means of hematoxylin&#8211;eosin staining&#46; Therefore&#44; immunohistochemical staining for tryptase and&#47;or c-kit &#40;CD 117&#41; is recommended&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Although TMEP has been considered to be a form of mastocytosis that only affects the skin&#44; it can cause systemic symptoms&#44; such as hypotension&#44; flushing&#44; pruritus&#44; abdominal pain&#44; and anaphylaxis due to the release of mediators by mast cells&#46; In other cases&#44; it can lead to symptoms caused by the infiltration of other organs&#44; such as splenomegaly&#44; adenopathy&#44; hepatomegaly&#44; and anemia&#46; Finally&#44; in isolated cases&#44; this variant of mastocytosis has been associated with myeloproliferative&#44; lymphoproliferative&#44; and myelodysplastic syndromes&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">The choice of treatment depends on whether systemic or exclusively cutaneous involvement is detected&#46; Cases involving only the skin have been treated satisfactorily with topical and intralesional corticosteroids&#44; topical calcineurin inhibitors&#44; 585<span class="elsevierStyleHsp" style=""></span>nm vascular laser treatment&#44; and psoralen-UV-A &#40;PUVA&#41; therapy&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflicts of Interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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        "texto" => "<p id="par0075" class="elsevierStylePara elsevierViewall">The authors would like to thank Jes&#250;s Cuevas Santos and Luis Cristian Perna Monroy for providing the histopathological images&#46;</p>"
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Article information
ISSN: 15782190
Original language: English
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2020 September 51 15 66
2020 August 23 21 44
2020 July 32 20 52
2020 June 31 26 57
2020 May 29 24 53
2020 April 42 27 69
2020 March 43 23 66
2020 February 6 7 13
2020 January 4 5 9
2019 December 8 9 17
2019 November 4 2 6
2019 October 0 5 5
2019 September 4 10 14
2019 August 4 13 17
2019 July 7 11 18
2019 June 4 7 11
2019 May 7 25 32
2019 April 4 22 26
2019 March 0 11 11
2019 February 4 0 4
2019 January 1 4 5
2018 December 2 0 2
2018 November 2 0 2
2018 October 3 0 3
2018 September 2 0 2
2018 July 0 2 2
2018 April 0 13 13
2018 February 52 10 62
2018 January 89 10 99
2017 December 87 9 96
2017 November 61 10 71
2017 October 56 4 60
2017 September 52 1 53
2017 August 103 11 114
2017 July 62 11 73
2017 June 82 44 126
2017 May 68 20 88
2017 April 70 10 80
2017 March 73 31 104
2017 February 67 11 78
2017 January 54 22 76
2016 December 75 18 93
2016 November 101 23 124
2016 October 151 12 163
2016 September 210 14 224
2016 August 97 11 108
2016 July 75 12 87
2016 June 13 15 28
2016 May 8 15 23
2016 April 2 1 3
2016 March 11 23 34
2016 February 2 19 21
2016 January 12 19 31
2015 December 7 10 17
2015 November 35 23 58
2015 October 32 17 49
2015 September 8 9 17
2015 August 8 5 13
2015 July 120 10 130
2015 June 70 9 79
2015 May 115 17 132
2015 April 75 10 85
2015 March 57 11 68
2015 February 43 11 54
2015 January 45 12 57
2014 December 46 9 55
2014 November 47 7 54
2014 October 64 17 81
2014 September 57 9 66
2014 August 55 14 69
2014 July 101 15 116
2014 June 70 12 82
2014 May 92 14 106
2014 April 76 9 85
2014 March 71 16 87
2014 February 70 13 83
2014 January 61 15 76
2013 December 27 4 31
2013 November 37 8 45
2013 October 17 3 20
2013 September 12 5 17
2013 August 9 8 17
2013 July 11 10 21
2013 June 10 13 23
2013 May 17 11 28
2013 April 7 8 15
2013 March 18 4 22
2013 February 23 2 25
2013 January 27 7 34
2012 December 11 3 14
2012 November 2 3 5
2012 October 1 1 2
2012 August 1 0 1
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Idiomas
Actas Dermo-Sifiliográficas
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¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?