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2.
Australas J Dermatol ; 64(1): 122-125, 2023 Feb.
Article in English | MEDLINE | ID: mdl-36484685

ABSTRACT

The external ear is a crucial part of the ear's anatomy for both functional and aesthetic purposes. We present a defect after the extirpation of an invasive squamous cell carcinoma, where the final defect involved the superior third of the outer ear, missing both cartilage and skin. The regional chondrocutaneous composite transposition flap of the ipsilateral auricular concha is a one-stage technique that successfully preserves the helical rim's shape and size.


Subject(s)
Ear Auricle , Ear Neoplasms , Plastic Surgery Procedures , Humans , Ear Neoplasms/surgery , Surgical Flaps , Ear, External/surgery , Ear Auricle/surgery
3.
Australas J Dermatol ; 63(3): e218-e221, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35622898

ABSTRACT

The COVID-19 pandemic led to a decrease in the number of operating rooms available. Single-stage islanded forehead flaps have emerged as a good alternative to the classic frontal flap helping to diminish the surgical waiting list. We present our case series of 6 patients reconstructed with islanded forehead flaps between February and July 2020.The purpose of this report is to assess the advantages and disadvantages of this technique in order to inform which subgroup of patients may benefit from the one-stage flap, now the pandemic is better controlled.


Subject(s)
COVID-19 , Rhinoplasty , Forehead , Humans , Nose/surgery , Pandemics , Rhinoplasty/methods
4.
Nature ; 589(7842): 448-455, 2021 01.
Article in English | MEDLINE | ID: mdl-33328637

ABSTRACT

FAT1, which encodes a protocadherin, is one of the most frequently mutated genes in human cancers1-5. However, the role and the molecular mechanisms by which FAT1 mutations control tumour initiation and progression are poorly understood. Here, using mouse models of skin squamous cell carcinoma and lung tumours, we found that deletion of Fat1 accelerates tumour initiation and malignant progression and promotes a hybrid epithelial-to-mesenchymal transition (EMT) phenotype. We also found this hybrid EMT state in FAT1-mutated human squamous cell carcinomas. Skin squamous cell carcinomas in which Fat1 was deleted presented increased tumour stemness and spontaneous metastasis. We performed transcriptional and chromatin profiling combined with proteomic analyses and mechanistic studies, which revealed that loss of function of FAT1 activates a CAMK2-CD44-SRC axis that promotes YAP1 nuclear translocation and ZEB1 expression that stimulates the mesenchymal state. This loss of function also inactivates EZH2, promoting SOX2 expression, which sustains the epithelial state. Our comprehensive analysis identified drug resistance and vulnerabilities in FAT1-deficient tumours, which have important implications for cancer therapy. Our studies reveal that, in mouse and human squamous cell carcinoma, loss of function of FAT1 promotes tumour initiation, progression, invasiveness, stemness and metastasis through the induction of a hybrid EMT state.


Subject(s)
Cadherins/deficiency , Epithelial-Mesenchymal Transition/genetics , Gene Deletion , Neoplasm Metastasis/genetics , Neoplasms/genetics , Neoplasms/pathology , Adaptor Proteins, Signal Transducing/metabolism , Animals , Cadherins/genetics , Cadherins/metabolism , Carcinoma, Squamous Cell/genetics , Carcinoma, Squamous Cell/pathology , Disease Progression , Enhancer of Zeste Homolog 2 Protein/metabolism , Epithelial Cells/metabolism , Epithelial Cells/pathology , Epithelial-Mesenchymal Transition/drug effects , Gene Expression Regulation, Neoplastic , Humans , Hyaluronan Receptors/metabolism , Lung Neoplasms/genetics , Lung Neoplasms/pathology , Mesoderm/metabolism , Mesoderm/pathology , Mice , Neoplasm Metastasis/drug therapy , Neoplasms/drug therapy , Neoplastic Stem Cells/metabolism , Neoplastic Stem Cells/pathology , Phenotype , Phosphoproteins/analysis , Phosphoproteins/metabolism , Proteomics , SOXB1 Transcription Factors/metabolism , Signal Transduction , Skin Neoplasms/genetics , Skin Neoplasms/pathology , Transcription Factors/metabolism , YAP-Signaling Proteins , Zinc Finger E-box-Binding Homeobox 1/metabolism , src-Family Kinases/metabolism
8.
Madrid; Academia Española de Dermatologia y Venereología; 2 oct. 2018. 40 p.
Non-conventional in Spanish | BIGG - GRADE guidelines | ID: biblio-1177471

ABSTRACT

El carcinoma de células de Merkel (CM) es un tumor cutáneo infrecuente (0.28 (95% CI: 0.15-0.40) casos por 100 000 personas año) y agresivo. El diagnóstico inicial y el estadiaje presentan variabilidad, y las técnicas a emplear podrían no estar disponibles en todos los centros. Por otro lado, la baja incidencia dificulta en muchos centros el poder adquirir experiencia. Existen guías de práctica clínica para el cuidado del CM, pero en contextos diferentes y con una cobertura parcial de los problemas que los dermatólogos han identificado como principales. Por ello, la Fundación Piel Sana AEDV, ha impulsado la adaptación de Guías de Práctica Clínica (GPC) sobre el CM, formando parte del proyecto Libro Blanco del Cáncer Cutáneo. El objetivo de esta guía es mejorar la calidad asistencial de los pacientes con CM, utilizando recomendaciones adaptadas a nuestro medio y basadas en los datos más válidos posibles. Esta guía revisa las principales técnicas diagnósticas empleadas en el diagnóstico inicial y estadiaje, así como los procedimientos terapéuticos para los tumores localizados.


Subject(s)
Humans , Middle Aged , Carcinoma, Merkel Cell/diagnosis , Carcinoma, Merkel Cell/prevention & control , Carcinoma, Merkel Cell/drug therapy
10.
Dermatol Ther ; 28(1): 40-3, 2015.
Article in English | MEDLINE | ID: mdl-25314592

ABSTRACT

Kaposi's sarcoma (KS) is an angioproliferative disorder caused by human herpesvirus 8 (HHV-8). Current research efforts have focused on the study of the relative role of KSHV-encoded genes in Kaposi's sarcomagenesis in order to identify novel mechanism-based therapies for patients suffering from this tumor. Although several viral genes have potential for KS pathogenesis, compelling data point to the KSHV-encoded G protein-coupled receptor (vGPCR) as a leading candidate viral gene for the initiation of KS. Interestingly, the oncogenic potential of vGPCR seems to correlate with its capacity to activate the mammalian target of rapamycin (mTOR) signaling pathway. Rapamycin, the prototypical inhibitor of the mTOR signaling pathway, has recently emerged as an effective treatment for KS when administered orally. In this case report, we present an immunocompetent patient with KS lesions treated with topical rapamycin achieving clinical and histologic healing after 16 weeks of treatment. The topical application of rapamycin could be a novel therapeutic option for the treatment of KS.


Subject(s)
Antibiotics, Antineoplastic/therapeutic use , Sarcoma, Kaposi/drug therapy , Sirolimus/therapeutic use , Skin Neoplasms/drug therapy , Administration, Cutaneous , Aged , Antibiotics, Antineoplastic/administration & dosage , Antibiotics, Antineoplastic/pharmacology , Humans , Male , Sarcoma, Kaposi/pathology , Sirolimus/administration & dosage , Sirolimus/pharmacology , Skin Neoplasms/pathology , Treatment Outcome
11.
Lasers Med Sci ; 30(7): 2009-14, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25359622

ABSTRACT

Several reports have shown the effectiveness of pulsed dye laser (PDL) for the treatment of basal cell carcinoma (BCC). Most studies have focused on low-risk BCCs, but an important limitation has been the lack of histologic confirmation of the treatment results. The aim of this study was to assess the effectiveness of PDL in high-risk BCCs with complete histologic evaluation with Mohs micrographic surgery (MMS). Seven patients with high-risk BCCs located on the face were included. All tumors were treated with three sessions of PDL (595 nm) at 4-week intervals. The tumor and 4 mm of peripheral skin were treated with two stacked pulses with a 1-s delay, a fluence of 15 J/cm(2), a pulse duration of 2 ms, and a spot size of 7 mm. MMS was performed at least 1 month after the last PDL session including excisional tumor debulking prior to the first stage of MMS for standard histologic evaluation. Apparent complete clinical response was achieved in five of seven patients. MMS was finally performed in six patients, and clear margins were achieved after one stage of MMS. The histologic evaluation of the tumor debulking specimens showed complete clearance in four of six cases. One patient who did not undergo MMS showed a recurrence after 14 months. This is the first pilot study that demonstrates that PDL can be effective for the treatment of high-risk BCCs. Until further scientific evidence is available, treatment of high-risk BCCs should include histologic confirmation of clearance.


Subject(s)
Carcinoma, Basal Cell/surgery , Lasers, Dye/therapeutic use , Skin Neoplasms/surgery , Aged , Aged, 80 and over , Carcinoma, Basal Cell/pathology , Face/pathology , Female , Humans , Male , Middle Aged , Mohs Surgery , Pilot Projects , Skin/pathology , Skin Neoplasms/pathology , Treatment Outcome
12.
Adv Ther ; 31(9): 945-60, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25145549

ABSTRACT

The incidence of malignant melanoma is increasing worldwide. In Spain, its incidence is increasing faster than any other cancer type, with a 5-year survival rate of about 85%. The impact and characteristics of malignant melanoma in the Spanish population can be ascertained from the national melanoma registry of the Academia Española de Dermatología y Venereología. This review presents consensus group recommendations for the diagnosis, staging and treatment of malignant melanoma in Spain. Incidence and mortality are discussed, as well as evaluation of various prevention and treatment strategies. Prognostic factors, such as BRAF and C-KIT mutations, which are expected to become routine staging procedures over the next few years, are outlined, especially in relation to treatment options. The use of recently approved targeted agents such as ipilimumab, a cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) inhibitor, and vemurafenib, a BRAF inhibitor, in metastatic disease are also discussed.


Subject(s)
Antibodies, Monoclonal/therapeutic use , Antineoplastic Agents/therapeutic use , Indoles/therapeutic use , Melanoma/drug therapy , Melanoma/pathology , Sulfonamides/therapeutic use , Humans , Incidence , Ipilimumab , Melanoma/diagnosis , Melanoma/genetics , Molecular Targeted Therapy , Mutation , Neoplasm Staging , Prognosis , Proto-Oncogene Proteins B-raf/genetics , Proto-Oncogene Proteins c-kit/genetics , Spain/epidemiology , Vemurafenib
18.
Actas dermo-sifiliogr. (Ed. impr.) ; 94(8): 503-523, oct. 2003. ilus, tab, graf
Article in Es | IBECS | ID: ibc-24826

ABSTRACT

La cirugía de Mohs es una técnica quirúrgica que permite la extirpación en capas de tumores cutáneos seleccionados con los más elevados porcentajes de curación. Al mismo tiempo permite el máximo ahorro de tejido sano. Todo ello es posible gracias a la supervisión microscópica, que posibilita analizar el 100% de los bordes tumorales de cada una de las capas y así poder guiar al cirujano en las sucesivas persistencias tumorales hasta la completa extirpación del tumor. Esta técnica tiene una gran aceptación en Estados Unidos, donde cerca del 30% de todos los epiteliomas son intervenidos con cirugía de Mohs, y poco a poco va adquiriendo protagonismo en Europa. Se revisan todos los aspectos de la técnica, el abordaje tumoral, las alternativas de tratamiento, las variantes de la técnica y las innovaciones más importantes. Se hace especial hincapié en las indicaciones, algunas ya consolidadas y otras no tanto, que cada día van aumentando en número debido a las ventajas de la técnica (AU)


Subject(s)
Humans , Skin Neoplasms/surgery , Mohs Surgery/methods , Risk Factors , Carcinoma, Basal Cell/surgery , Neoplasm Recurrence, Local/prevention & control , Skin Neoplasms/ultrastructure
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