Sílvia Planas

ORCID: 0000-0003-1509-1681
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Fetal and Pediatric Neurological Disorders
  • Prenatal Screening and Diagnostics
  • Tumors and Oncological Cases
  • Sarcoma Diagnosis and Treatment
  • Cardiac tumors and thrombi
  • Gastrointestinal disorders and treatments
  • Cardiac Structural Anomalies and Repair
  • Chromosomal and Genetic Variations
  • Pediatric Hepatobiliary Diseases and Treatments
  • Testicular diseases and treatments
  • Soft tissue tumor case studies
  • Oral Health Pathology and Treatment
  • Autoimmune and Inflammatory Disorders
  • Blood disorders and treatments
  • Thermal Regulation in Medicine
  • Tuberous Sclerosis Complex Research
  • Teratomas and Epidermoid Cysts
  • Cardiomyopathy and Myosin Studies
  • Eosinophilic Disorders and Syndromes
  • Appendicitis Diagnosis and Management
  • Immune Cell Function and Interaction
  • Bone Tumor Diagnosis and Treatments
  • Cytomegalovirus and herpesvirus research
  • Congenital Anomalies and Fetal Surgery
  • Immunodeficiency and Autoimmune Disorders

Hospital Universitari de Vic
2025

Anthrologica
2024

Hospital Sant Joan de Déu Barcelona
2021-2024

Universitat de Barcelona
2018

Southmead Hospital
2017

North Bristol NHS Trust
2017

Sheffield Children's NHS Foundation Trust
2014-2015

Vall d'Hebron Hospital Universitari
2012

Bristol Royal Infirmary
2012

Universitat Autònoma de Barcelona
2003-2009

Abstract Necrotizing fasciitis (NF) is a severe bacterial soft tissue infection primarily affecting muscle fascia and subcutaneous tissue. In Europe, it has an annual incidence of 3–5 cases/100 000, with mortality rate 10–15% (rising to 38–45% in septic shock). Risk factors include hypertension, immunosuppression, diabetes, obesity trauma. NF commonly occurs the extremities perineal region less frequently chest. monomicrobial cases, Streptococcus pyogenes most identified. Treatment involves...

10.1093/bjs/znaf024.033 article EN British journal of surgery 2025-02-01

Fetal primary cardiac tumors (FPCTs) are very rare. The majority of them correspond to rhabdomyomas, followed by other benign neoplasms or hamartomas. We describe the case a third trimester female stillborn with an incidental autopsy finding Hamartoma Mature Cardiac Myocytes (HMCM), rare tumor previously unreported in fetal neonatal period. intrauterine demise occurred at 32 + 6 weeks gestation after uneventful pregnancy. revealed structurally normal heart small subendocardial nodule just...

10.1177/10935266241286716 article EN Pediatric and Developmental Pathology 2024-09-28

To evaluate the correlation of periventricular echogenic halo (halo sign) with histopathological findings and its association other brain imaging abnormalities in fetuses cytomegalovirus (CMV) infection.

10.1002/uog.26173 article EN Ultrasound in Obstetrics and Gynecology 2023-02-02

Cytotoxic T-lymphocyte antigen-4 (CTLA-4) haploinsufficiency is a T-cell hyperactivation disorder that can manifest with both immunodeficiency and immune dysregulation. Approximately one-third of patients may present mild symptoms remain stable under supportive care. The remaining develop severe multiorgan autoimmunity requiring lifelong immunosuppressive treatment. Hematopoietic stem cell transplantation (HSCT) potentially curable for treatment-resistant Nevertheless, little experience...

10.3389/fimmu.2022.1070068 article EN cc-by Frontiers in Immunology 2022-12-27

Therapeutic hypothermia (TH) after neonatal encephalopathy, commonly provided by 72 hours of whole-body cooling using a wrap, limits parents' physical contact with their infants affecting bonding and may not be suitable for encephalopathic preterm fragile skin. Alternative methods are unavailable this population. We investigated in pig model the feasibility achieving 3.5°C reduction rectal temperature (Trectal) similar to clinical TH protocols from 38.5°C (normothermia pigs) target 35°C ±...

10.1089/ther.2017.0028 article EN Therapeutic Hypothermia and Temperature Management 2017-10-23

An otherwise healthy eight‐year‐old girl presented with a mass in the soft tissue of sacral region. The lesion was diagnosed as vascular malformation on imaging studies, for which percutaneous sclerotherapy attempted. continued to grow and complete resection performed after four years. pathological diagnosis giant cell ependymoma (GCE). GCE is term used describe rare histologic variant characterized by malignancy‐like morphologic phenotype indolent behavior. To best our knowledge, this first...

10.1111/neup.12713 article EN Neuropathology 2021-02-10

10.1111/ced.13354 article EN Clinical and Experimental Dermatology 2017-12-28

Abstract Two male siblings with several malformations are reported. The anomalies detected in both fetuses were mesomelic camptomelia, postaxial hexadactyly and Dandy–Walker complex. There was only one similar previous report the literature. This combination could represent a specific pattern of malformation or new syndrome, different variants. parents' consanguinity recurrence subsequent pregnancy suggest an autosomal recessive inheritance pattern. Copyright © 2003 John Wiley & Sons, Ltd.

10.1002/pd.601 article EN Prenatal Diagnosis 2003-03-31

A previously healthy 3-year-old boy was referred by his general practitioner to the paediatric outpatient clinic because of a 6-month history moderate severe constipation. It associated with mild central abdominal pain and slight weight loss. He had been treated Movicol, minimal effect. There …

10.1136/archdischild-2014-306648 article EN Archives of Disease in Childhood Education & Practice 2014-08-11

1. Figure 1 shows an abnormal bowel gas distribution with central paucity, and the impression that is displaced into upper abdomen. 2. Figure 2 a large fluid-filled mass occupying most of abdomen but not extending above liver (arrowed) subphrenic space. This was initially erroneously reported as gross ascites. 3. Figure 3 septated cystic abdominal mass, no discernible cyst wall. Its maximum dimensions are 18.5×10.5×23.5 cm (transverse × antero-posterior cranio-caudal diameters). 4. The...

10.1136/archdischild-2014-306648a article EN Archives of Disease in Childhood Education & Practice 2015-05-18

A 3-year-old girl with no relevant medical or family history presented five small asymptomatic, indurated cutaneous nodules in the left lumbar region. The first two lesions were noticed 18 months prior to consultation. Six before presentation, three new developed same Physical examination showed an agminated group of brown, nodules, from 3 6 mm diameter (Figures 1 and 2). Laboratory tests normal negative including a complete blood count, circulating autoantibodies infectious studies. An...

10.1111/pde.15390 article EN Pediatric Dermatology 2023-07-26

Periventricular hyperechogenicity “halo” sign, is one of the most frequent US abnormalities in CMV-infected fetuses. It has been defined as a sign ventriculitis and white matter injury. However, there are few reports about postmortem targeted histological examination. Our objective was to obtain more information its significance prognostic value. Two experienced pathologists reviewed slides central nervous system (CNS) from 26 fetuses following termination pregnancy 2nd (N=19) or 3rd...

10.1002/uog.23884 article EN Ultrasound in Obstetrics and Gynecology 2021-10-01
Coming Soon ...