Esther Moreno-Moreno

ORCID: 0000-0003-4422-9897
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About
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Research Areas
  • Breast Cancer Treatment Studies
  • Genetic factors in colorectal cancer
  • Autoimmune Bullous Skin Diseases
  • Vasculitis and related conditions
  • Endometrial and Cervical Cancer Treatments
  • Renal Diseases and Glomerulopathies
  • Breast Lesions and Carcinomas
  • Urologic and reproductive health conditions
  • Lymphoma Diagnosis and Treatment
  • Cardiac Structural Anomalies and Repair
  • Cancer Diagnosis and Treatment
  • Soft tissue tumor case studies
  • CNS Lymphoma Diagnosis and Treatment
  • Autoimmune and Inflammatory Disorders Research
  • Genetic Neurodegenerative Diseases
  • Hedgehog Signaling Pathway Studies
  • Chronic Kidney Disease and Diabetes
  • Oral health in cancer treatment
  • Salivary Gland Tumors Diagnosis and Treatment
  • Metastasis and carcinoma case studies
  • Mitochondrial Function and Pathology
  • Renal Transplantation Outcomes and Treatments
  • Chromatin Remodeling and Cancer
  • Cardiac tumors and thrombi
  • Reproductive tract infections research

Instituto Cajal
2021-2025

Instituto Ramón y Cajal de Investigación Sanitaria
2025

Hospital Universitario Ramón y Cajal
2018-2023

Universidad de Granada
1995

Background: Characterisation of molecular alterations pleomorphic lobular carcinoma (PLC), an aggressive subtype invasive (ILC), have not been yet completely accomplished. Methods: To investigate the with features, a total 39 tumour samples (in situ and lesions lymph node metastases) from 27 patients nuclear grade 3 carcinomas were subjected to morphological, immunohistochemical massive parallel sequencing analyses. Results: Our observations indicated that features morphologically...

10.3390/cancers11010074 article EN Cancers 2019-01-11

Secondary haemophagocytic lymphohistiocytosis (sHLH) is characterised by a hyper activation of immune system that leads to multiorgan failure. It suggested excessive response in patients with COVID-19 could mimic this syndrome. Some autopsy studies have revealed the presence haemophagocytosis images bone marrow, raising possibility, along HScore parameters, sHLH.Our objective ascertain existence sHLH some severe COVID-19.We report histological findings 16 COVID-19, focusing on obtained from...

10.1136/jclinpath-2020-207337 article EN Journal of Clinical Pathology 2021-03-15

HER2 antibody-drug conjugates like Trastuzumab deruxtecan (TDxd) have shown efficacy in HER2-low cancers, however the prevalence and clinical impact of endometrial cancer (EC) remains unclear. This study investigates expression EC, focusing on frequency, its distribution across histologic molecular subtypes, intratumoral heterogeneity, prognostic significance. retrospective analysis included EC patients categorized histologically molecularly, using ASCO/CAP scoring guidelines for...

10.1016/j.ygyno.2025.02.005 article EN cc-by-nc-nd Gynecologic Oncology 2025-02-12

In this study, we developed a quantitative method with digital image analysis to evaluate the degree of gingival overgrowth (GO), and compared GO in kidney transplant patients treated cyclosporin A (CsA) (n = 21) or CsA+nifedipine 8) group healthy controls 30). The was reproducible reliable. Our findings showed significant differences papillary surface between inducers. Gingival index also differed significantly each patient (p < 0.01, Kruskal-Wallis test). administration calcium channel...

10.1111/j.1600-051x.1995.tb00810.x article EN Journal Of Clinical Periodontology 1995-08-01

Abstract Background Immunohistochemistry (IHQ) is commonly used for the detection of mismatch repair proteins deficiency (MMRD). One very infrequent abnormal pattern MMR protein expression loss PMS2 and MSH6, with intact MLH1 MSH2. Case presentation We review frequency this MMRD IHC among 108 colorectal (CRCs) 35 endometrial cancers in our files at least one protein, present two CRCs showing MSH6 (1.9% CRCs). NGS analysis these tumours identified mutations (R134* germline mutation tumour M1R...

10.1186/s13000-020-01001-2 article EN cc-by Diagnostic Pathology 2020-07-14

Abstract Background: Virilism is a female disorder in which secondary male sexual characteristics develop, caused by an excessive adrenal or ovarian androgen secretion. Case presentation: Here, we report unusual case of steroid cell tumor, not otherwise specified (NOS), 68-year-old who presented with androgenic alopecia, clitoromegaly and increased muscle mass. Laboratory investigations revealed both hyperandrogenism elevation precursors mimicking congenital hyperplasia. A left adnexal mass...

10.1515/dx-2018-0007 article EN Diagnosis 2018-05-12

Secondary syphilis is a polymorphic condition resulting from the hematogenous and lymphatic dissemination of Treponema pallidum. Human immunodeficiency virus-positive patients are in greater risk atypical severe forms disease. The most common manifestation generalized papulosquamous eruption with variable mucosal involvement. However, annular plaques, split commissural papules, crusted necrotic or ulcerated lesions also frequent. Granulomatous lesions, both clinically histologically, less...

10.1177/0956462419869136 article EN International Journal of STD & AIDS 2019-09-27

In this study, molecular alterations in endometrial carcinoma (EC) recurrences were analyzed. We aimed to identify genes implicated tumor progression and evaluate whether histologic type shifting occurs recurrences. Thus, we analyzed 50 samples corresponding 24 primary ECs (15 low-grade endometrioid carcinomas [LG-EECs] 9 high-grade carcinomas) their 26 These studied by immunohistochemistry, next-generation sequencing, MLH1 promoter methylation. observed shared mutations all tumors...

10.1097/pas.0000000000002308 article EN The American Journal of Surgical Pathology 2024-09-13

Proliferative fasciitis (PF) is a benign fibroblastic reaction with histological and clinical characteristics that overlap those of malignant soft tissue tumors; thus, it referred to as pseudosarcomatous reaction. It continues be an important cause diagnostic error overtreatment. The childhood PF subtype has some distinct immunohistochemical make differential diagnosis tumors even harder, especially sarcoma. These proliferations generally occur in the lower limbs, periorbital region rare...

10.1080/01676830.2021.1973513 article EN Orbit 2021-09-02

Understanding the role of donor-specific antibodies (DSAs) in liver transplantation remains an investigative priority. Acute and chronic rejection associated with DSAs have been described. However, most transplant protocols did not consider presence at moment (LTx) or for follow-up. A 65-year-old man received ABO-compatible LTx cirrhosis. Ten years after LTx, he presented a progressive elevation enzymes bilirubin. The single antigen Luminex bead assay showed against several DQ2, DQ7, DQ8...

10.3390/transplantology2010001 article EN cc-by Transplantology 2021-01-03

La ataxia de Friedreich es una enfermedad neurodegenerativa progresiva transmisión autosómica recesiva, que conforma la hereditaria más frecuente en nuestro medio. Se produce por expansión 33 repeticiones del triplete GAA, secundaria a mutación cromosoma 9q13. manifiesta antes los 25 años con síntomas neurológicos, locomotores, endocrinológicos y cardiológicos, siendo estos últimos marcan el pronóstico. esperanza vida 40-50 años. Existen medicamentos pretenden mejorar detener progresión...

10.37536/riecs.2017.2.1.2 article ES cc-by Revista de Investigación y Educación en Ciencias de la Salud (RIECS) 2017-03-22

Perineal carcinoma of unknown primary origin (CUP) is a rare entity and represents diagnostic therapeutic challenge. These tumors may respond well to combination surgical resection, when feasible, local radiotherapy, platinum-based systemic chemotherapy. A 67-year-old male patient consulted for urinary discomfort associated with perineal abscess. The abscess was drained, the diagnosed origin. Computed tomography (CT) scan shows large mass that involves both corpora cavernosa corpus...

10.31487/j.scr.2021.01.15 article EN Surgical Case Reports 2021-01-28

Ampullary adenocarcinoma (AA) can originate from three different epitheliums, conditioning its evolution and prognosis. Recently, histomolecular classification has been defined, according to the presence of immunohistochemical (IHQ) markers intestinal (INT) lineage vs pancreatobiliary (PB). 42 AA patients were retrospectively reviewed morphologically molecular classified with IHQ MUC1, MUC2, CDX2, CK20 CK7 markers, system described by Chang et al. A prognostic study was carried out in...

10.1016/j.soda.2021.100023 article EN cc-by-nc-nd Surgery Open Digestive Advance 2021-09-01

Castleman’s disease is a rare lymphoproliferative disorder. The localized form the most frequent and it usually asymptomatic. Although definitive diagnosis histologic, necessary to know how manifests in imaging studies. location cases of unicentric thorax. We present case patient from our center improve interpretation proof this pathology.

10.32440/ar.2021.138.03.cc01 article EN ANALES RANM 2021-01-01
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