Júlia Costa Linhares

ORCID: 0000-0002-2651-0610
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About
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Research Areas
  • Cancer Diagnosis and Treatment
  • Ovarian cancer diagnosis and treatment
  • Glioma Diagnosis and Treatment
  • Genetic factors in colorectal cancer
  • Neuroblastoma Research and Treatments
  • Colorectal and Anal Carcinomas
  • Colorectal Cancer Treatments and Studies
  • Teratomas and Epidermoid Cysts
  • Ovarian function and disorders
  • Pituitary Gland Disorders and Treatments
  • Oral and Maxillofacial Pathology
  • Genomic variations and chromosomal abnormalities
  • Bone Tumor Diagnosis and Treatments
  • Colorectal Cancer Screening and Detection
  • Sarcoma Diagnosis and Treatment
  • Women's cancer prevention and management
  • Assisted Reproductive Technology and Twin Pregnancy
  • Cancer and Skin Lesions
  • Lymphoma Diagnosis and Treatment
  • Academic Research in Diverse Fields
  • Reproductive Biology and Fertility
  • Soft tissue tumor case studies
  • Gastrointestinal Tumor Research and Treatment
  • Metastasis and carcinoma case studies
  • Endometrial and Cervical Cancer Treatments

Hospital Erasto Gaertner
2023-2024

Universidade Federal do Paraná
2023-2024

Faculdade Evangélica do Paraná
2024

Gaertner (United States)
2023-2024

Hospital Universitário Evangélico de Curitiba
2022-2023

Universidade Positivo
2023

Background Congenital immature orbital teratomas are rare neoplasms, with intraorbital cases presenting unique diagnostic and therapeutic challenges. Case presentation This report presents a patient that exhibited rapid-growing right exophthalmos since birth. Imaging studies revealed progressively expanding lesion in the cavity optic nerve. Following partial resection subsequent exenteration, histopathological immunohistochemical analyses confirmed diagnosis of teratoma sarcomatous...

10.52783/jns.v14.1605 article EN Journal of Neonatal Surgery 2025-02-07

ABSTRACT BACKGROUND: Microscopic analysis of tumor budding (TB) may be an essential predictive tool for regional lymph node metastases in colorectal cancer, especially among patients intermediate stages, who exhibit considerable prognostic variability. AIMS: The aim this study was to assess the power BT regarding presence and its association with other characteristics related carcinoma progression. METHODS: This is a cross-sectional, retrospective quantitative approach, focusing on review...

10.1590/0102-6720202500006e1875 article EN cc-by ABCD Arquivos Brasileiros de Cirurgia Digestiva (São Paulo) 2025-01-01

ABSTRACT BACKGROUND: Part of colorectal cancer cases occurs due to modifications in the DNA mismatch repair system, which are responsible for microsatellite instability. This alteration results an unconventional phenotypic pattern cancer. AIMS: To describe epidemiological, histopathological and molecular profiles patients with who underwent surgical treatment a reference hospital. METHODS: is cross-sectional, retrospective study quantitative approach, that included review patients’ medical...

10.1590/0102-672020230053e1771 article EN cc-by ABCD Arquivos Brasileiros de Cirurgia Digestiva (São Paulo) 2023-01-01

Introduction/Background: Pediatric diffuse midline gliomas are predominantly localized within the brainstem, pons, or bi-thalamic, while in adolescents and adults, they arise unilaterally thalamus spinal cord. Epidemiological data remain scarce for this recently described entity. They represent 10-15% of all pediatric brain tumors 75% brainstem tumors. Case presentation: Herein we report a case Diffuse Midline Glioma 10-year-old male patient, with an unusual location cord, presenting...

10.46900/apn.v6i2.246 article EN cc-by Archives of Pediatric Neurosurgery 2024-05-01

Introdução: Sarcomas do estroma endometrial são raros, originando-se no tecido de sustentação das glândulas endometriais. Classificam-se em baixo grau (SEEBG), alto e indiferenciado. Os SEEBGs, agressivos, costumam apresentar sintomas, como sangramento uterino anormal, dor pélvica dismenorreia. Relato caso: Mulher 44 anos, inicialmente diagnosticada com leiomioma epitelioide; dois anos mais tarde, avaliação histopatológica, o mioma pariu, sugerindo SEEBG. Histerectomia total confirmou...

10.5327/jbg-2965-3711-2024134101 article PT Jornal Brasileiro de Ginecologia 2024-01-01

Introduction: Leiomyosarcomas (LMS) are rare malignant neoplasms originating in smooth muscle, more common women their fifth and sixth decades of life. Inherent characteristics the retroperitoneum allow LMS this location to reach substantial proportions present symptoms only advanced stages. Case report: A 37-year-old woman sought medical attention July 2020 due growth a painful, fixed mass left hemiabdomen that appeared six months earlier. The patient denied urinary or gastrointestinal...

10.32635/2176-9745.rbc.2024v70n1.4592 article EN cc-by Revista Brasileira de Cancerologia 2024-04-24

Introduction: American data show that about 30% of thyroidectomies are performed due to a diagnosis cancer. With regard the Brazilian scenario, information regarding profile thyroidectomized patients is scarce. Objectives: To carry out an epidemiological survey and catalog histopathological submitted thyroidectomy in 11 years. Methods: Retrospective observational study with collections through medical records system variables sex, age, surgical approach, characteristics lesions...

10.55684/2024.82.e016 article EN cc-by-sa BioSCIENCE 2024-05-12

Introdução: O tumor de células granulares (TCG) é uma neoplasia rara e predominantemente benigna, frequentemente localizada na região da cabeça pescoço. Comumente, afeta adultos entre 40 60 anos, com maior incidência em mulheres. TCG mamário, representando 5% a 15% todos os TCG, demanda diagnóstico histopatológico virtude semelhanças clínicas radiológicas malignidades mamárias. Tipicamente, manifesta-se como massa solitária palpável, embora multicentricidade ocorra até 20% dos casos, seja...

10.32635/2176-9745.rbc.2024v70n2.4609 article PT cc-by Revista Brasileira de Cancerologia 2024-06-04

Introdução: Struma ovarii é um tipo raro de tumor ovário com comportamento usualmente benigno; apesar disto, uma minoria pode sofrer malignização, sendo que quando isto ocorre, o mais comum se dê na forma carcinoma papilífero tireoide. O curso clínico costuma ser insidioso, e ao exame histopatológico, observa-se tecido tireoidiano maduro associado à coexistência tireoide características nucleares típicas. Relato caso: presente relato descreve caso struma maligno em paciente do sexo feminino...

10.30928/2527-2039e-20243688 article PT Relatos de Casos Cirúrgicos do Colégio Brasileiro de Cirurgiões 2024-06-28

Abstract Background Since the FDA approved immune-enhancing therapies for patients with high microsatellite instability (MSI-H) and/or mismatch repair deficiency (dMMR), recognizing these biomarkers in solid tumors has gained clinical importance. Although MSI-H and dMMR are considered uncommon breast cancer, previous studies on bilateral cancer (biBC) identified a surprisingly frequency of MSI. Methods In this study, we aimed to describe prevalence its association clinicopathologic...

10.1186/s42047-024-00156-2 article EN cc-by Surgical and Experimental Pathology 2024-08-09

Breast cancer is the most common among women, with 5 to 15% of these cases classified as invasive lobular carcinoma (ILC). Metastases can occur at any stage disease, sites being bones, lungs, lymph nodes, liver, and brain. However, extragenital metastasis uterus rare. This study describes a case 52-year-old woman breast pain for over month. Mammography indicated suspicious nodule (BIRADS 5). Physical examination revealed nodule, peau d’orange skin, axillary mass. Core biopsy diagnosed...

10.29289/259453942024015 article EN Mastology 2024-01-01

O carcinossarcoma é uma neoplasia maligna mista, de origem epitelial e mesenquimal, que ocorre em qualquer topografia do trato genital feminino inferior, mais frequentemente no útero. pico incidência torno dos setenta anos idade, essencialmente mulheres afrodescendentes período pós-menopausa. presente estudo visa relatar um caso paciente 65 correlacionar os achados com a literatura científica. Devido à agressividade tumor, baixa taxa sobrevida, prognóstico infausto dificuldade clínica...

10.55684/80.2.36 article PT cc-by-sa BioSCIENCE 2022-11-01

Introdução: O linfoma é uma neoplasia maligna originada de proliferação anormal linfócitos que pode acometer gânglios linfáticos ou outros órgãos. Esta entidade representa cerca 5% das doenças oncológicas e ser classificada em: Hodgkin não Hodgkin. primário gastrointestinal raro, representando 10% a 20% dos casos extranodal. Sua principal origem nas células B, sendo o subtipo difuso grandes B (LDGCB) forma mais frequente. Os acometidos, normalmente, são do sexo masculino após os 55 anos....

10.53843/bms.v8i12.549 article PT cc-by Brazilian Medical Students 2023-09-05

Introdução: Struma ovarii é um tipo raro de tumor ovariano composto por mais 50% tecido tireoidiano. Representa apenas 1% dos tumores sólidos do ovário e 3% subtipos dermoides, com a maioria casos curso benigno. Geralmente afeta mulheres entre terceira quinta décadas vida, sendo muitas vezes assintomático ou sinais inespecíficos. A síndrome pseudo-Meigs, caracterizada ascite derrame pleural, pode estar presente, dificultando o diagnóstico. Relato caso: Mulher, 43 anos, desconforto abdominal,...

10.32635/2176-9745.rbc.2023v69n4.4177 article PT cc-by Revista Brasileira de Cancerologia 2023-09-29

Introduction: Breast carcinomas are the major cause of death in women with cancer worldwide, mainly metastatic cases. The pituitary gland stands for only 6-8% secondary sites distant metastasis and it is usually asymptomatic. When symptomatic, these lesions can mimic primary diseases. Case report: A 43-year-old woman underwent a left mastectomy axillary lymph node dissection April 2013 due to luminal, invasive ductal carcinoma nodal metastasis. Six years later, she started complaining...

10.32635/2176-9745.rbc.2023v69n4.4212 article EN cc-by Revista Brasileira de Cancerologia 2023-10-03
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