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1.
Actas Dermosifiliogr ; 2024 Jun 12.
Article in English, Spanish | MEDLINE | ID: mdl-38876209

ABSTRACT

INTRODUCTION: In 2017, the Spanish Academy of Dermatology and Venereology Psoriasis Working Group (PWG) designed the Minimal Disease Activity (MDA) criteria to determine the level of disease activity. We hereby present the results of an observational, cross-sectional, multicenter study of the nationwide application of these criteria. MATERIAL AND METHODS: We conducted a non-randomized sampling, stratified to achieve autonomic and provincial representation of consecutive patients with psoriasis (Ps) vulgaris without active arthritis. A total of 830 patients were included: 493 men (59.5%), with a mean age of 51.4 years (SD, 14.2), from all autonomous regions of Spain (except for Ceuta and Melilla) and 44 (88%) out of the 50 provinces. A questionnaire was obtained with demographic data, DLQI, subjective assessment-on a scale from 0 to 10-of itching, erythema, desquamation, visibility, and the patients' PASI and BSA. RESULTS: More than 50% failed to meet the MDA criteria (491; 59.2%), with significant differences being reported by region, sex, and age. Additionally, significant differences were reported based on the therapy used (P<.001). The use of biological therapies was associated with higher MDA compliance compared to other therapies (59.4% vs 23.3%). No differences were reported among various biological therapies. CONCLUSIONS: The overall rate of MDA compliance is low, with differences being based on geographic location, sex, age, and drug used, yet none of these factors separately justify them.

2.
Arch Dermatol Res ; 311(5): 369-376, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30955082

ABSTRACT

The interaction of lectin-like transcript 1 (LLT1) with CD161 inhibits Natural Killer cell activation. Overexpression of LLT1 contributes to the immunosuppressive properties of tumor cells. However, there are little data about LLT1 expression in human solid tumors. The objective of this paper is to investigate the relationship between LLT1 expression with the clinicopathologic features and its impact on the prognosis of head and neck cutaneous squamous cell carcinoma (cSCC). LLT1 expression was analyzed on paraffin-embedded tissue samples obtained from 100 patients with cSCC by immunohistochemistry. The estimator of Fine and Gray was used to estimate the cumulative incidence curves for relapse. Proportional Hazard models and Hazard ratios (HRs) were used for studying the risk of tumor relapse and mortality. LLT1 strong expression was a significant risk factor for nodal metastasis with crude and adjusted ratios (HRs) of 3.40 (95% CI 1.39-9.28) and 3.25 (95% CI 1.15-9.16); and for cSCC specific death of 6.17 (95% CI 1.79-21.2) and 6.10 (95% CI 1.45-25.7). Strong LLT1 expression is an independent predictor of nodal metastasis and poor disease-specific survival and it might be helpful for risk stratification of patients with cSCC.


Subject(s)
Biomarkers, Tumor/metabolism , Lectins, C-Type/metabolism , Lymphatic Metastasis/pathology , Receptors, Cell Surface/metabolism , Skin Neoplasms/pathology , Squamous Cell Carcinoma of Head and Neck/pathology , Aged , Aged, 80 and over , Disease-Free Survival , Feasibility Studies , Female , Humans , Incidence , Kaplan-Meier Estimate , Male , Neoplasm Recurrence, Local/diagnosis , Neoplasm Recurrence, Local/epidemiology , Prognosis , Risk Assessment/methods , Risk Factors , Skin/pathology , Skin Neoplasms/mortality , Squamous Cell Carcinoma of Head and Neck/mortality
3.
Lupus ; 26(12): 1328-1332, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28387637

ABSTRACT

Objective The objective of this report is to independently validate the adjusted Global Antiphospholipid Syndrome Score (aGAPSS) to predict thrombosis in a cohort of patients with APS and/or autoimmune disease. Methods This retrospective cohort study included 319 consecutive patients with APS and/or autoimmune disease. Data on clinical manifestations, conventional cardiovascular risk factors and aPL profile were collected. The aGAPSS was calculated for each patient by adding together the points corresponding to the risk factors. Results Among the 319 patients included (mean age: 48.0; SD 15.47), conducted over a mean period of 52 months (range: 19-394), 219 fulfilled the current APS classification criteria (PAPS diagnosed in 130 patients and APS associated autoimmune disease (aAPS) in 89 patients), and 100 patients with autoimmune disease without APS (AD). A total of 201 patients (63.0%) had a history of one or several thrombotic manifestations, 189 (86.3%) of them APS patients: 118 PAPS (mean age: 50.14; SD 15.47) and 71 aAPS (mean age: 48.13; SD 15.81). Higher aGAPSS baseline values were seen in patients with thrombosis 6.58 (SD 3.36) when compared with those without 4.90 (SD 4.33) ( p = 0.001). Conclusions This study has shown that even when anti-phosphatidylserine/prothrombin antibodies (aPS/PT) are not computed in an adjusted model of GAPSS (aGAPSS), this score represents an improvement in assessment of the risk prediction of thrombosis in APS patients and/or autoimmune disease. However, cut-off values may differ from other kinds of cohorts, which suggests that baseline characteristics in divergent groups of patients can account for differences in cut-off values of GAPSS.


Subject(s)
Antiphospholipid Syndrome/complications , Autoimmune Diseases/complications , Risk Assessment/methods , Thrombosis/etiology , Adult , Antibodies, Antiphospholipid/immunology , Antiphospholipid Syndrome/immunology , Autoimmune Diseases/immunology , Cohort Studies , Female , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors
4.
J Eur Acad Dermatol Venereol ; 31(2): 241-246, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27592851

ABSTRACT

BACKGROUND: Sentinel lymph node biopsy and wide local excision of the primary melanoma (SLNB) is now a standard staging procedure for patients with melanomas 1 mm or more in thickness, but its therapeutic benefit is not clear. OBJECTIVE: To determine whether there is an association between performance of SLNB and patient prognosis. METHODS: Studies assessing the association between performance of SLNB and patient prognosis were pooled from MEDLINE, EMBASE, PubMed, Cochrane Database of Systematic Reviews and Google Scholar. From each study, first author's last name, publication year, origin country, type of study design, characteristics of participants and the Hazard risk (HR) for melanoma specific survival (MSS) with the corresponding 95% confidence interval (95% CI) were collected. Methodological assessment of the studies was evaluated using the Newcastle-Ottawa scale (NOS) and the 'Risk of bias' tool detailed in the Cochrane Handbook for Systematic Reviews of Interventions. Meta-analyses for the global HR were performed. In addition, in order to explore the sources of heterogeneity among the studies, sensitivity analyses are also provided. RESULTS: A total of six studies with 8764 patients who had undergone SLNB and 11054 patients who had undergone wide location excision alone (WLEA) were identified for the analysis. The indicators suggest that the heterogeneity is low: τ2  = 0; H = 1 [1; 1.74]; I2  = 0% [0%; 66.5%]. Evidence for publication bias was not found (Egger's test P = 0.4654). The pooled MSS HR from fixed effects analysis was determined to be 0.88 (95% CI = 0.80-0.96). CONCLUSIONS: Although no significant survival difference was observed in four of the six series, the pooling summary data from all the studies that deal with this issue suggested that SLNB is associated with a significantly better outcome compared with WLEA for localized melanoma.


Subject(s)
Melanoma/pathology , Melanoma/surgery , Sentinel Lymph Node Biopsy/methods , Skin Neoplasms/pathology , Skin Neoplasms/surgery , Humans , Prognosis
5.
J Perinatol ; 35(10): 803-8, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26181721

ABSTRACT

OBJECTIVE: To evaluate the impact of management of childbirth (external cephalic version (ECV) plus planned vaginal delivery (PVD)) of breech presentation at term (⩾37 weeks of gestation). STUDY DESIGN: This retrospective cohort study was based on data collected of singleton breech presentations at term in the Obstetrics and Gynaecology Service, Cruces University Hospital (Biscay, Spain), from January 2003 to December 2012. RESULT: We attended 2377 singleton breech pregnancies at term. We attended 1684 singleton breech term deliveries, attempting vaginal delivery after selection in 52.9% of cases and were successful in 57.5% of attempts. A total of 1360 ECV were attempted, with a success rate of 50.3% of those attempted. The use of ECV has decreased the rate of breech presentation at delivery by 39.0%, the rate of breech presentation as a caesarean section (CS) indication by 47.1% (CS due to breech presentation/total of CS) and the rate of CS for breech presentation out of the total of deliveries by 39.1% (CS due to breech presentation/total of deliveries). Early postnatal parameters (5-min Apgar score, umbilical cord arterial pH and acid-base analysis) were significantly lower following PVD compared with planned CS for breech presentation. However, we did not find any differences in the rates of admissions to the neonatal unit or neonatal mortality. CONCLUSION: Management of breech presentation with a protocol that includes ECV, careful selection criteria and active management of vaginal delivery achieve a great decrease in the rate of CS for breech presentation.


Subject(s)
Breech Presentation/therapy , Cesarean Section/statistics & numerical data , Infant Mortality , Term Birth , Version, Fetal/methods , Version, Fetal/statistics & numerical data , Adult , Disease Management , Female , Humans , Infant , Infant, Newborn , Pregnancy , Pregnancy Outcome , Retrospective Studies , Spain
6.
BJOG ; 121(2): 230-5; discussion 235, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24245964

ABSTRACT

OBJECTIVE: To determine if external cephalic version (ECV) can be performed with safety and efficacy in women with previous caesarean section. DESIGN: Prospective comparative cohort study. SETTING: Cruces University Hospital (Spain). POPULATION: Single pregnancy with breech presentation at term. METHODS: We compared 70 ECV performed in women with previous caesarean section with 387 ECV performed in multiparous women (March 2002 to June 2012). MAIN OUTCOME MEASURES: Success rate, complications of the ECV and caesarean section rate. RESULTS: The success rate of ECV in women after previous caesarean section was 67.1% versus 66.1% in multiparous women (P = 0.87). The logistic regression analysis confirmed this result (odds ratio 0.93, 95% CI 0.52-1.68; P = 0.82) adjusted by the variables associated with success of ECV. There were no complications in the previous caesarean section cohort. The vaginal delivery rate in the previous caesarean section cohort was 52.8% versus 74.9% in the multiparous cohort (P < 0.01). There were no cases of uterine rupture. CONCLUSION: Based on our data, we conclude that complications are uncommon with ECV in women with previous caesarean section, with a success rate comparable to that of multiparous women. Uterine scar should not be considered a contraindication and ECV should be offered to women with previous caesarean section with breech presentation at term.


Subject(s)
Cesarean Section , Term Birth , Version, Fetal , Breech Presentation , Cardiotocography , Contraindications , Female , Humans , Logistic Models , Parity , Pregnancy , Prospective Studies , Pulmonary Edema/etiology , Uterine Hemorrhage/etiology , Vaginal Birth after Cesarean/statistics & numerical data
7.
Leukemia ; 27(11): 2149-56, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23579575

ABSTRACT

Adult acute myeloid leukemia (AML) is a highly heterogeneous stem cell malignancy characterized by the clonal expansion of immature myeloid precursors. AML may emerge de novo, following other hematopoietic malignancies or after cytotoxic therapy for other disorders. Here, we investigated the clonal vs reactive nature of residual maturing bone marrow cells in 59 newly diagnosed adult AML and mixed phenotype acute leukemia (MPAL) patients as assessed by interphase fluorescence in situ hybridization analysis of AML and myelodysplastic syndrome-associated cytogenetic alterations and/or the pattern of chromosome X inactivation, in females. In addition, we investigated the potential association between the degree of molecular/genetic involvement of hematopoiesis and coexistence of altered immunophenotypes by flow cytometry. Our results indicate that residual maturing neutrophils, monocytes and nucleated red cell precursors from the great majority of newly diagnosed AML and MPAL cases show a clonal pattern of involvement of residual maturing hematopoietic cells, in association with a greater number of altered immunophenotypes. These findings are consistent with the replacement of normal/reactive hematopoiesis by clonal myelopoiesis and/or erythropoiesis in most newly diagnosed AML and MPAL cases, supporting the notion that in most adults presenting with de novo AML, accumulation of blast cells could occur over a pre-existing clonal hematopoiesis.


Subject(s)
Bone Marrow/pathology , Hematopoiesis , Leukemia, Biphenotypic, Acute/pathology , Leukemia, Myeloid, Acute/pathology , Adult , Aged , Bone Marrow/immunology , Female , Follow-Up Studies , Humans , Immunophenotyping , In Situ Hybridization, Fluorescence , Karyotyping , Leukemia, Biphenotypic, Acute/genetics , Leukemia, Biphenotypic, Acute/immunology , Leukemia, Myeloid, Acute/genetics , Leukemia, Myeloid, Acute/immunology , Male , Middle Aged , Mutation/genetics , Polymerase Chain Reaction , Prognosis , Proto-Oncogene Proteins c-kit/genetics
8.
J Eur Acad Dermatol Venereol ; 26(6): 785-8, 2012 Jun.
Article in English | MEDLINE | ID: mdl-21569114

ABSTRACT

BACKGROUND: Several studies stated that patient with psoriasis carried an increased risk of psoriasis but some studies did not demonstrate this association. OBJECTIVES: The aim of this study was to evaluate the prevalence of hypertension in psoriasis based on a sample of Spanish population. METHODS: This was a hospital-based case-control study involving 661 psoriatic patients (cases) and 661 control matched by gender and age. Meta-analysis of the previous studies was made. RESULTS: The prevalence of hypertension was significantly higher in psoriasis patients than controls (30.3%, 21.3%, respectively, P < 0.001). In a multivariate analysis, hypertension was associated with psoriasis after controlling for age, gender, diabetes, obesity and smoking (OR = 1.44, 95% confidence interval: 1.07-1.94). CONCLUSION: The results of this study support the association between psoriasis and hypertension.


Subject(s)
Hypertension/complications , Psoriasis/complications , Adult , Case-Control Studies , Female , Humans , Hypertension/epidemiology , Male , Middle Aged , Multivariate Analysis , Prevalence
9.
Dermatology ; 222(2): 109-12, 2011.
Article in English | MEDLINE | ID: mdl-21304243

ABSTRACT

Imiquimod is an immunomodulator of the imidazoquinoline group which possesses antiviral and antitumour activities. Although its mechanism of action has not been entirely elucidated yet, imiquimod 5% cream has been shown to be an efficient, long-lasting and safe therapy for multiple actinic keratoses in non-immunosuppressed patients and in transplant recipients. We report the case of a 44-year-old patient with a third renal transplant who developed an acute tubular necrosis confirmed by renal biopsy after the use of imiquimod 5% cream. The result of a literature search revealed a wide variety of side effects attributable to the use of imiquimod.


Subject(s)
Acute Kidney Injury/chemically induced , Aminoquinolines/adverse effects , Interferon Inducers/adverse effects , Kidney Transplantation/adverse effects , Warts/drug therapy , Acute Kidney Injury/diagnosis , Acute Kidney Injury/therapy , Adult , Aminoquinolines/therapeutic use , Creatinine/blood , Humans , Imiquimod , Interferon Inducers/therapeutic use , Male , Renal Dialysis , Treatment Outcome , Warts/virology
14.
Rev. venez. endocrinol. metab ; 7(3): 10-15, sep. 2009. tab
Article in Spanish | LILACS-Express | LILACS | ID: lil-631357

ABSTRACT

Objetivos: Determinar la frecuencia de las anormalidades del descenso testicular y los factores asociados en recién nacidos (RN). Métodos: Se realizó un estudio clínico observacional tipo caso control. Durante el período noviembre 2007- Agosto 2008, se examinaron en el Instituto Autónomo Hospital Universitario de los Andes (IAHULA) todos los RN con criptorquidia, los cuales se compararon con 105 RN sin criptorquidia (grupo control). Datos complementarios fueron obtenidos mediante una encuesta a los padres. Resultados: De un total de 2084 RN, 35 presentaron criptorquidia, lo cual corresponde a una frecuencia del 1,7%. La criptorquidia ocurrió en 10,8% de los RN pre-término y solamente en 0,8 % de los RN de término. La prematuridad y el bajo peso al nacer se asociaron con mayor frecuencia con la criptorquidia (p<0,05). Otros factores como la talla, el índice Apgar y la longitud del pene de los RN, también estuvieron asociados con la presencia de criptorquidia. El riesgo relativo indirecto (Odds ratio) de presentar criptorquidia es 5,27 veces mayor en un RN pre-término comparado con un RN de término. Los RN con malformaciones congénitas tienen un riesgo 7,03 veces mayor de tener criptorquidia que un RN sin malformaciones congénitas. Conclusiones: Se confirma que en nuestros niños la criptorquidia es más frecuente en RN pre-término y que la frecuencia de criptorquidia en RN es del 1,7%. El bajo peso al nacer, la prematuridad, el pene de pequeñas dimensiones junto con la presencia de anomalías congénitas asociadas, son factores que se relacionan con el mal descenso testicular.


Objectives: To establish the frequency of abnormalities of testicular descent and associated factors in newborn (NB) boys. Methods: An observational clinical study, case control type, was performed. All criptorchydic NB were evaluated at the Hospital Universitario de Los Andes, from November 2007 to August 2008. They were compared with 105 NB without cryptorchidism. A survey to obtain data from the patients, and their parents was conducted. Results: Criptorchidism was present in thirty five out of 2084 male newborns, representing 1.7% of the sample. In preterm NB, the frecuency of criptory was 10.8%, compared to 0.8% frequency observed in at term male newborns. Prematurity and low birth weight were associated with increased frequency of chryptorchidism (p<0,05). Newborns height, Apgar index, and the lenght of their penis, were also associated with increased presence of chryptorchidism. The calculated odds ratio risk for criptorchidism is 5.27 times higher in pre-term NB compared to term boys at birth. The risk for chriptorchidism in a newborns with morphological developmental abnormalities, is 7.03 times higher than in a NB without such abnormalities. Conclusions: We have verified that criptorchidism in our children is more frequent in pre-term newborns, and that 1.7% is the frequency of criptorchidism in this sample. Low birth weight, prematurity, and the small penis dimensions, together with associated morphological developmental abnormalities, are risk factors related to abnormal testicular descent.

16.
Actas dermo-sifiliogr. (Ed. impr.) ; 99(4): 301-304, mayo 2008. ilus, tab
Article in Es | IBECS | ID: ibc-63049

ABSTRACT

El hamartoma o nevus oligemicus es una entidad infrecuente, de etiopatogenia poco aclarada, en la que se produce una vasoconstricción selectiva del plexo vascular profundo dérmico con relación al superficial. Estas alteraciones funcionales dan lugar a lesiones fijas, adquiridas y asintomáticas a modo de máculas lívidas, eritematosas, típicamente frías al tacto si se compara con la piel sana adyacente. Comunicamos los casos de 6 varones jóvenes con lesiones en el abdomen y en los flancos, compatibles clínicamente con nevus oligemicus. La medición de la temperatura superficial de la lesión, constatando un descenso de hasta 2,5 °C respecto de la piel sana adyacente, permitió realizar el diagnóstico definitivo. Se describen los estudios complementarios realizados, los diagnósticos diferenciales, los posibles agentes etiológicos responsables y se comentan los casos referidos en la literatura hasta el momento. Consideramos que el nevus oligemicus es una entidad infradiagnosticada y mucho más frecuente de lo referido en la literatura (AU)


Hamartoma or nevus oligemicus is an uncommon lesion that is characterized by selective vasoconstriction of the deep dermal vascular plexus with respect to the superficial one and whose cause has not been clearly established. This selective vasoconstriction gives rise to fixed, acquired, and asymptomatic lesions in the form of livid, erythematous macules that are typically cold to touch compared with surrounding skin. We report the cases of 6 young men with lesions clinically compatible with nevus oligemicus on the abdomen and flanks. Measurement of the surface temperature of the lesion revealed a decrease of up to 2.5 °C with respect to healthy surrounding skin and allowed a definitive diagnosis to be made. We describe the additional studies undertaken, the differential diagnosis, and the possible etiologic agents, and discuss the cases reported in the literature to date. In our opinion, nevus oligemicus is an underdiagnosed lesion that is much more common than has been reported in the literature (AU)


Subject(s)
Humans , Male , Adult , Middle Aged , Hamartoma/pathology , Nevus/pathology , Skin Neoplasms/pathology , Diagnosis, Differential
17.
Actas Dermosifiliogr ; 99(4): 301-4, 2008 May.
Article in Spanish | MEDLINE | ID: mdl-18394407

ABSTRACT

Hamartoma or nevus oligemicus is an uncommon lesion that is characterized by selective vasoconstriction of the deep dermal vascular plexus with respect to the superficial one and whose cause has not been clearly established. This selective vasoconstriction gives rise to fixed, acquired, and asymptomatic lesions in the form of livid, erythematous macules that are typically cold to touch compared with surrounding skin. We report the cases of 6 young men with lesions clinically compatible with nevus oligemicus on the abdomen and flanks. Measurement of the surface temperature of the lesion revealed a decrease of up to 2.5 degrees C with respect to healthy surrounding skin and allowed a definitive diagnosis to be made. We describe the additional studies undertaken, the differential diagnosis, and the possible etiologic agents, and discuss the cases reported in the literature to date. In our opinion, nevus oligemicus is an underdiagnosed lesion that is much more common than has been reported in the literature.


Subject(s)
Hamartoma/diagnosis , Skin Diseases/diagnosis , Adult , Humans , Male , Middle Aged
18.
Rev. venez. endocrinol. metab ; 5(2): 1-2, jun. 2007. ilus, graf, tab
Article in Spanish | LILACS-Express | LILACS | ID: lil-631239
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