36 results match your criteria: "Nova Hospital[Affiliation]"

Background: Antibiotic therapy is currently considered a safe and effective treatment alternative for computed tomography (CT)-confirmed uncomplicated acute appendicitis with recent studies reporting good results on both oral antibiotics only and outpatient management. Furthermore, there are promising pilot results on uncomplicated acute appendicitis management with symptomatic treatment (placebo). This trial aims to assess whether both antibiotics and hospitalization can be safely omitted from the treatment of uncomplicated acute appendicitis.

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Hydrocele of the Canal of Nuck: A report of five cases.

Int J Surg Case Rep

October 2023

Department of Emergency Medicine, Nova Hospital, Kailali, Nepal. Electronic address:

Introduction And Importance: Canal of Nuck hydrocele is a rare condition in females. Due to mild symptoms, it may be neglected, leading to complications, including infection and bleeding. The rarity of this condition, coupled with its potential for adverse outcomes, necessitates a high index of suspicion among treating surgeons to diagnose and promptly manage the case.

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Introduction And Importance: Ileal perforation is a rare but serious condition that can arise from accidental ingestion of foreign objects. This report discusses an unusual case of ileal perforation peritonitis caused by ingestion of a chicken bone.

Case Presentation: A 60-year-old male presented with acute generalized abdominal pain, fever, nausea, and vomiting for three days.

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Tuberous sclerosis (TSC) is an autosomal dominant neurocutaneous disorder. This case highlights rare isolated neurologic finding in a TSC patient emphasizing the need for heightened suspicion even in the absence of any cutaneous findings and family history.

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Aggressive thoracic hemangiomas are rare, benign tumors that extend into the spinal canal and cause neurological symptoms. Delayed diagnosis and treatment, due to a paucity of literature on optimal treatment strategies, can increase morbidity. This case report describes a 19-year-old male patient with aggressive thoracic hemangioma who presented with upper back pain and progressive weakness of the lower extremities.

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Article Synopsis
  • - Scrub typhus, caused by the bacteria Orientia tsutsugamushi, typically doesn't lead to neurological issues, but can result in rare cases of intracerebral bleeding, especially in endemic areas.
  • - A case study reported a 40-year-old woman with left-sided weakness and fever linked to scrub typhus; imaging showed a hematoma in her brain along with other organ issues, requiring intensive medical intervention.
  • - The case highlights the importance of considering serious neurological complications in scrub typhus patients, even if they're rare, to ensure timely and effective treatment.
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Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort.

Fam Cancer

November 2024

Applied Tumor Genomics, Research Programs Unit, University of Helsinki, Biomedicum Helsinki Haartmaninkatu 8), PO Box 63, 00014, Helsinki, Finland.

Article Synopsis
  • About 50% of Finnish Lynch Syndrome cases are linked to a specific variant in the MLH1 gene, resulting from a deletion in exon 16 caused by recombination.* -
  • The study validated this variant in a population cohort from FinnGen and the Central Finland Biobank, comparing cancer rates and onset age between those with and without the variant.* -
  • They found that out of 348 potential variant carriers, a significant portion had cancer or a family history of cancer, highlighting the potential of large genetic studies for detecting hereditary cancer risks.*
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Background: Lynch syndrome (LS) is an autosomal dominant multi-organ cancer syndrome with a high lifetime risk of cancer. The number of cumulative colorectal adenomas in LS does not generally exceed ten, and removal of adenomas via routine screening minimizes the cancer burden. However, abnormal phenotypes may mislead initial diagnosis and subsequently cause suboptimal treatment.

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Introduction And Importance: Encysted spermatic cord hydrocele is a rare anomaly characterized by obstruction of processus vaginalis closure. Clinically, it presents as a swelling in the inguinal region extending to the upper scrotum and does not communicate with the peritoneal cavity. It is often mistaken for indirect inguinal hernias, inguinal lymphadenopathy, undescended testis, and primary tumors of the cord in infants and children, making the diagnosis challenging.

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Introduction And Importance: Bipolar fractures involving segmental fractures of the lateral and proximal clavicles are exceptionally rare, with only isolated cases documented in the literature. Such fractures may easily be overlooked during the initial presentation.

Case Presentation: We present the case of a 35-year-old male with deformation in the middle segment of the clavicle following a road traffic accident (RTA).

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Introduction And Importance: Isolated pancreatic injury following blunt abdominal trauma is rare, and the absence of definite clinical signs and symptoms may delay diagnosis and management.

Case Presentation: We present the case of a seven-year-old girl with a history of progressive, periumbilical abdominal pain and multiple episodes of non-bilious, non-blood mixed vomiting following a road traffic accident. Computed tomography (CT) imaging revealed an isolated grade three pancreatic injury managed conservatively.

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Background: Intramedullary tibial nailing (IMN) is the gold standard for stabilizing tibial shaft fractures. IMN can be performed through an infra- or suprapatellar approach.

Purpose: The aim of this study is to compare the rate of fasciotomies for acute compartment syndrome between infra- and suprapatellar approaches.

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Background: Hemangioma is a common benign tumor resulting from abnormal blood vessel growth but is infrequent in the breast. Preoperatively, it is challenging to diagnose breast hemangioma using clinical and conventional imaging modalities because of their lack of pathognomonic characteristics. An excisional biopsy can be used for tissue diagnosis in cases of diagnostic uncertainty.

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Infantile Epileptic Spasms Syndrome (IESS) is an epileptic encephalopathy in childhood that affects infants under the age of two years. When spasm series occur, prognosis for cognitive outcome is poor in the majority of cases. The encephalopathy in IESS includes delayed maturation of normal sleep phenomena in the EEG, such as sleep spindles.

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Introduction And Importance: Osteochondromas, the most common benign tumors of the appendicular skeleton, are uncommonly found in the spine. Although the cervical spine is the most frequent location of spinal osteochondromas, the lower cervical spine is less commonly affected.

Case Presentation: We present the case of a 16-year-old female adolescent who presented with a hard palpable mass over the nape of the neck more toward the right side associated with non-radiating pain for 3 years.

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Introduction: The hydrocele of the canal of Nuck is a rare cause of bilateral inguino-labial swelling. Due to its rarity, lack of clinician knowledge regarding this entity, and paucity of relevant literature, it can be misdiagnosed and often mistreated.

Case Presentation: We present a case of a two-year-old female with bilateral inguino-labial swelling who was diagnosed with a hydrocele of the canal of Nuck based on history and clinical examination.

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Unlabelled: Lynch syndrome (LS) is the most common hereditary cancer syndrome. Early diagnosis improves prognosis and reduces health care costs, through existing cancer surveillance methods. The problem is finding and diagnosing the cancer predisposing genetic condition.

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Splenic cysts are classified on the basis of epithelial lining, either primary or secondary. Primary cysts are further divided as parasitic and nonparasitic. The secondary cysts are usually post traumatic or after a splenic extension of pancreatic pseudocyst.

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Lynch Syndrome Genetics and Clinical Implications.

Gastroenterology

April 2023

Department of Surgery, Helsinki University Hospital, Helsinki, Finland; Applied Tumor Genomics Research Programs Unit, University of Helsinki, Helsinki, Finland; Faculty of Medicine and Health Technology, Tampere University and Tays Cancer Center, Tampere University Hospital, Tampere, Finland.

Lynch syndrome (LS) is one of the most prevalent hereditary cancer syndromes in humans and accounts for some 3% of unselected patients with colorectal or endometrial cancer and 10%-15% of those with DNA mismatch repair-deficient tumors. Previous studies have established the genetic basis of LS predisposition, but there have been significant advances recently in the understanding of the molecular pathogenesis of LS tumors, which has important implications in clinical management. At the same time, immunotherapy has revolutionized the treatment of advanced cancers with DNA mismatch repair defects.

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Is HLA type a possible cancer risk modifier in Lynch syndrome?

Int J Cancer

May 2023

Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Article Synopsis
  • Lynch syndrome (LS) is the most prevalent inherited cancer syndrome linked to DNA mismatch repair (MMR) gene variants and poses a 30% to 80% risk of various cancers for carriers.
  • The condition leads to the buildup of frameshift mutations that create immunogenic peptides, which may affect how the immune system recognizes and responds to MMR-deficient cancers.
  • The INDICATE initiative has been launched to investigate how a LS carrier's HLA genotype could influence cancer risk, enhance understanding of immune responses, and direct future research on genetically defined risk populations.
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Guideline for the treatment of no light perception eyes induced by mechanical ocular trauma.

J Evid Based Med

September 2022

Evidence-based Medicine Center, School of Basic Medical Sciences, Lanzhou University, Lanzhou, P. R. China.

Article Synopsis
  • Severe eye injuries that cause no light perception usually mean a bad chance of seeing again, and doctors might need to remove the eye.
  • New surgical techniques have made it better for patients with these serious injuries, but there are still no clear rules on when and how to perform the surgery.
  • To help, experts created guidelines with 16 recommendations to improve how doctors diagnose and treat these severe eye injuries.
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Article Synopsis
  • - A patient experienced fatigue and a pulling sensation in his lower legs, along with continuous muscle contractions in his trunk (known as myokymia).
  • - These symptoms suggested a diagnosis of Isaacs syndrome, a rare neuromuscular condition.
  • - The diagnosis was confirmed through blood tests that showed a strong presence of CASPR2 antibodies.
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Purpose: Recent studies have reported alarming appendiceal tumor rates associated with complicated acute appendicitis, especially in patients presenting with a periappendicular abscess. However, the data on histology of appendiceal tumors among acute appendicitis patients is limited, especially in patient cohorts differentiating between uncomplicated and complicated acute appendicitis. We have previously reported the association of increased appendiceal tumor prevalence with complicated acute appendicitis in this population-based study.

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Cataract surgery via phacoemulsification with intraocular lens (IOL) placement in the capsular bag is the gold standard in the presence of adequate capsular support. However, when capsule and/or zonular fibers are weak or absent, alternate fixation strategies are required. Common alternative options include retropupillary iris-claw IOLs (RP-IC IOLs) and scleral-fixated IOLs (SF IOLs).

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