María Pilar Sánchez-Salas

Centro de Salud Casa del Barco

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Co-Authors

F.J. Carapeto

Cytodiagnostics (Canada)

J. Pérez-Pelegay

Hospital Clínico Universitario Lozano Blesa

Francisco Javier García Latasa de Aranibar

Centro de Salud Casa del Barco

F.J. García-Latasa de Aranibar

Universitat de Barcelona

J. J. Martin

RELX Group (Netherlands)

Purificación Ventura-Faci

Hospital Materno-Infantil

María Pilar Grasa

Hospital Clínico Universitario Lozano Blesa

Yolanda Gilaberte

Hospital Universitario Miguel Servet

A. Lázaro

Universidad de Zaragoza

M.A. Ania

Centro de Salud Casa del Barco

Cooperative Institutions

Hospital Clínico Universitario Lozano Blesa

Centro de Salud Casa del Barco

Hospital Universitario Miguel Servet

Universidad de Zaragoza

Hospital General San Jorge

Instituto de Investigación Sanitaria Aragón

Hospital Royo Villanova

GZA Ziekenhuizen Campus Sint-Augustinus

KU Leuven

Instituto Aragonés de Ciencias de la Salud

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Vitiligo-like lesions located over In-transit metastases of malignant melanoma as a clinical marker of complete response to pembrolizumab.

Dermatology Online Journal (2019)

Tamara Gracia‐Cazaña Esteban Padgett Alba Hernández-García María Pilar Sánchez-Salas

Anti-programmed cell death (PD)-1 therapies in metastatic tumors have a high incidence of immune adverse events, including cutaneous manifestations such as vitiligo-like lesions. This side effect is associated with increased survival and it is a clinical marker of response to treatment. This case report is a graphic representation of the appearance of vitiligo-like lesions over in-transit metastases of malignant melanoma linked to a complete response to treatment with pembrolizumab.

Vitiligo

10.5070/d32512046728

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Citations (2)

Telangiectasias de la piel y la mucosa oral

Piel (2008)

María Pilar Sánchez-Salas Francisco Javier García Latasa de Aranibar

10.1016/s0213-9251(08)70988-2

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Citations (2)

Acquired perforating dermatosis: clinicopathological study of 31 cases, emphasizing pathogenesis and treatment

Journal of the European Academy of Dermatology and Venereology (2017)

Ana Julia García‐Malinis E. Sánchez María Pilar Sánchez-Salas Eliodoro Del Prado C. Coscojuela

Acquired perforating dermatosis (APD) is a rare group of skin disorders of unknown aetiology and pathogenesis and is associated with several systemic diseases.We review the clinicopathological features, associated systemic diseases and treatment response in a series of APD patients.We conducted a retrospective observational study of all patients histologically diagnosed with APD in Hospital San Jorge (Huesca, Spain) between 2002 and 2014. Demographic and clinical features were collected from medical records. Statistical analyses were carried out using SPSS software (version 20.0; IBM Corp, Armonk, NY, USA).The study population consisted of 31 patients (19 women and 12 men), with a mean age of 54 years. Reactive perforating collagenosis (n = 15, 45%) was the most common histopathologic type. The most frequently affected area was the lower limbs (66.6%, n = 22), and pruritus was present in 19 patients (61.3%, P = 0.005). Arterial hypertension (30.3%) was the most common associated condition. Five patients were receiving treatment with infliximab when diagnosed with APD. Most patients responded to topical steroids and oral antihistamines (n = 15).This study is retrospective, and the sample size is limited.Acquired perforating dermatosis is an underdiagnosed dermatosis frequently associated with systemic disorders. Its pathogenesis may involve vascular damage, not only in patients with diabetes, but also in those with arterial hypertension and chronic venous insufficiency. Control of pruritus and underlying extracutaneous disorders, as well as discontinuation of the treatment with biologics, are important aspects of the management of this dermatosis.

Discontinuation

Etiology

Pathogenesis

Medical record

10.1111/jdv.14220

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Citations (71)

Lesiones psoriasiformes acrales

Actas Dermo-Sifiliográficas (2009)

María Pilar Sánchez-Salas F.J. García-Latasa de Aranibar M.A. Ania

10.1016/s0001-7310(09)70828-2

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Citations (0)

Lesión tumoral eritematosa en una pierna

Piel (2008)

María Pilar Sánchez-Salas Francisco Javier García Latasa de Aranibar Paula Gambó Grasa

10.1016/s0213-9251(08)70989-4

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Appearance of comedones at the site of healed herpes zoster: Wolf’s isotopic response

International Journal of Dermatology (2011)

María Pilar Sánchez-Salas

Subject matter

10.1111/j.1365-4632.2009.04439.x

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Citations (19)

Nódulo en el pabellón auricular

Piel (2006)

María Pilar Sánchez-Salas I. García-Salces

10.1016/s0213-9251(06)72442-x

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Citations (0)

Evolución cutánea atípica (tipo paquidérmico) de una mastocitosis

Actas Dermo-Sifiliográficas (2007)

María Pilar Sánchez-Salas A. Lázaro J. J. Martin María Pilar Grasa F.J. Carapeto

10.1016/s0001-7310(07)70164-3

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Citations (1)

Acral Psoriasiform Lesions

Actas Dermo-Sifiliográficas (2009)

María Pilar Sánchez-Salas F.J. García-Latasa de Aranibar M.A. Ania

The patient presented symmetrical, erythematousviolaceous plaques on the distal phalanges of the fingers and toes; the plaques had a hyperkeratotic and desquamative surface (Figures 1 and 2). There was also slight reddening and desquamation of the lobes of the ears. In addition, the patient was asthenic, with mild jaundice of the skin and mucosas, and presented hepatomegaly and palpable right lateral cervical lymph nodes that formed a mass of approximately 4 by 3 cm (Figure 3). Additional Tests

Desquamation

Phalanx

10.1016/s1578-2190(09)70071-x

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Unilateral progressive telangiectatic eruption with a metameral distribution during pregnancy

Journal of Obstetrics and Gynaecology (2016)

Lucía Prieto‐Torres Tamara Gracia‐Cazaña María Pilar Sánchez-Salas Gorka Muñiz Esteban Padgett

"Unilateral progressive telangiectatic eruption with a metameral distribution during pregnancy." Journal of Obstetrics and Gynaecology, 37(3), pp. 377–378

10.1080/01443615.2016.1244813

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