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What's new in your rare disease | Kisho

Not rare diseases news,
news about your rare disease.

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Research

A rare case study highlights the surgical and endovascular management of a mycotic common femoral artery pseudoaneurysm resulting from septic ankle arthritis. This case contributes to the understanding of complications arising from septic arthritis.

rare case of mycotic common femoral artery pseudoaneurysm from septic ankle arthritis surgical and endovascular considerations

PubMed Rare Disease·9 months ago·Read at source →

Original title: “A Rare Case of Mycotic Common Femoral Artery Pseudoaneurysm from Septic Ankle Arthritis: Surgical and Endovascular Considerations.”

autoimmune encephalitis autoimmune limbic encephalitisResearch

Recent research highlights the association of autoimmune encephalitis with anti-recoverin antibodies, providing insights into potential biomarkers for diagnosis. This discovery may enhance understanding and treatment strategies for affected patients.

autoimmune encephalitis associated with anti recoverin antibodies

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Autoimmune encephalitis associated with anti-recoverin antibodies.”

thyroid lymphoma gastric lymphoma+1 moreResearch

A recent study highlights the diagnostic challenges posed by benign thyroid nodules that can mimic residual disease in patients with concurrent thyroid and gastric diffuse large B-cell lymphoma. The research emphasizes the importance of ultrasound-guided biopsy for accurate diagnosis.

benign thyroid nodule mimicking residual disease on positron emission tomography computed tomography in a patient with concurrent thyroid and gastric diffuse large b cell lymphoma the value of ultrasound guided biopsy

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Benign thyroid nodule mimicking residual disease on positron emission tomography/computed tomography in a patient with concurrent thyroid and gastric diffuse large B-cell lymphoma: the value of ultrasound-guided biopsy.”

dengue diseaseResearch

A recent study evaluates the risks of dengue outbreaks on blood donation safety in Australia, extending beyond known outbreak areas. This research highlights the need for enhanced monitoring and safety protocols in blood donation practices.

assessing dengue outbreak risks to blood donation safety beyond significant outbreak areas in australia

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Assessing dengue outbreak risks to blood donation safety, beyond significant outbreak areas in Australia.”

acute myeloid leukemiaResearch

A recent study highlights the prognostic significance of myelodysplasia-related gene mutations in patients with FLT3-ITD-mutated acute myeloid leukemia. This research could influence treatment strategies and patient management in this specific leukemia subtype.

prognostic impact of myelodysplasia related gene mutations in flt3 itd mutated acute myeloid leukemia

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Prognostic impact of myelodysplasia-related gene mutations in FLT3-ITD-mutated acute myeloid leukemia.”

cancer esophageal cancerResearch

New research highlights the development of user-defined peptide libraries that enhance the sensitive detection of cancer antigens. This advancement could improve diagnostic capabilities in oncology.

sensitive detection of cancer antigens enabled by user defined peptide libraries

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Sensitive detection of cancer antigens enabled by user-defined peptide libraries.”

systemic sclerosis limited systemic sclerosis+1 moreResearch

Recent research indicates that targeting the PD-1 pathway may reduce inflammation and fibrosis in systemic sclerosis. This discovery could lead to new therapeutic strategies for managing this challenging condition.

engaging the pd 1 pathway in systemic sclerosis attenuates inflammation driven fibrosis

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Engaging the PD-1 pathway in systemic sclerosis attenuates inflammation-driven fibrosis.”

posterior leukoencephalopathy syndromeResearch

A case report details posterior reversible encephalopathy syndrome occurring with intracranial hemorrhage following split-liver transplantation. This finding contributes to the understanding of complications associated with liver transplants.

case report of posterior reversible encephalopathy syndrome with intracranial hemorrhage after split liver transplantation

PubMed Rare Disease·9 months ago·Read at source →

Original title: “A Case Report of Posterior Reversible Encephalopathy Syndrome With Intracranial Hemorrhage After Split-Liver Transplantation.”

Research

A recent publication explores the mechanisms and safety of statins in gastroenterology, highlighting human evidence supporting their use. This research may influence treatment strategies for gastrointestinal conditions.

statins in gastroenterology mechanisms human evidence and safety

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Statins in Gastroenterology: Mechanisms, Human Evidence, and Safety.”

pulmonary hypertension pulmonary hypertension, primary, 6+1 moreResearch

A recent study explores multimodality imaging insights in a rare adult survivor of Taussig-Bing heart with pulmonary hypertension. This research contributes to understanding the complexities of this rare congenital heart defect.

taussig bing heart with pulmonary hypertension in a rare adult survivor multimodality imaging insights

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Taussig-Bing heart with pulmonary hypertension in a rare adult survivor: multimodality imaging insights.”

bronchiectasisResearch

A study published in PubMed examines bronchiectasis characteristics in patients with various genotypes of severe α(1)-antitrypsin deficiency. The findings contribute to understanding the disease's impact on lung health.

characteristics of bronchiectasis in patients with different genotypes of severe 1 antitrypsin deficiency from the earco registry

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Characteristics of bronchiectasis in patients with different genotypes of severe α(1)-antitrypsin deficiency from the EARCO registry.”

Bardet-Biedl syndrome Bardet-Biedl syndrome 1+1 moreResearch

A novel protein truncating mutation in the TTC8 gene has been identified as the cause of Bardet-Biedl Syndrome in a Pakistani family. This discovery adds to the understanding of genetic factors contributing to BBS.

novel protein truncating mutation of ttc8 causes bardet biedl syndrome bbs in a pakistani family

PubMed Rare Disease·9 months ago·Read at source →

Original title: “A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.”

spinal cord sarcomaResearch

A multicenter study by the Korean Society of Spinal Tumors evaluates the feasibility and oncologic outcomes of en bloc resection with intentional tumor transgression in primary spinal sarcoma. This research contributes to understanding surgical approaches in treating this rare cancer.

feasibility and oncologic outcome of en resection with intentional tumor transgression in primary spinal sarcoma the korean society of spinal tumors multicenter study ksst 2024 02

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Feasibility and oncologic outcome of en resection with intentional tumor transgression in primary spinal sarcoma: The Korean Society of Spinal Tumors multicenter study (KSST 2024-02).”

adenoid cystic carcinoma esophageal adenoid cystic carcinoma+1 moreResearch

A recent case study highlights the diagnostic challenges and surgical management of adenoid cystic carcinoma of the larynx. The findings emphasize the need for long-term surveillance in patients to monitor for recurrence.

case of adenoid cystic carcinoma of the larynx diagnostic challenges surgical management and long term surveillance

PubMed Rare Disease·9 months ago·Read at source →

Original title: “A case of adenoid cystic carcinoma of the larynx: Diagnostic challenges, surgical management, and long-term surveillance.”

apolipoprotein A-II amyloidosisResearch

A recent study highlights the dual pathology of fibrillary glomerulonephritis and apolipoprotein A-IV amyloidosis, diagnosed using mass spectrometry and DNAJB9 immunohistochemistry. This research contributes to the understanding of these rare diseases and their diagnostic challenges.

fibrillary glomerulonephritis and apolipoprotein a iv amyloidosis a rare dual pathology diagnosed by mass spectrometry and dnajb9 immunohistochemistry

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Fibrillary Glomerulonephritis and Apolipoprotein A-IV Amyloidosis: A Rare Dual Pathology Diagnosed by Mass Spectrometry and DNAJB9 Immunohistochemistry.”

Research

A recent publication discusses a case study of multiple oral white papules in a 3-year-old girl, prompting further investigation into potential underlying conditions. This case highlights the importance of clinical quizzes in diagnosing rare presentations in pediatric patients.

multiple oral white papules in a 3 year old girl a quiz

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Multiple Oral White Papules in a 3-year-old Girl: A Quiz.”

carpal tunnel syndrome carpal tunnel syndrome 1+1 moreResearch

A recent study explores the clinical, surgical, and histopathological aspects of carpal tunnel syndrome in patients with mucopolysaccharidosis type I. The findings contribute to understanding the complications associated with this rare disease.

carpal tunnel syndrome in mucopolysaccharidosis type i clinical surgical and histopathological findings

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Carpal tunnel syndrome in mucopolysaccharidosis type I: clinical, surgical and histopathological findings.”

congenital temporomandibular joint ankylosis psoriasis+1 moreResearch

A rare case report highlights the association of temporomandibular joint ankylosis with psoriasis and familial Mediterranean fever. This finding may provide insights into the complex interplay between these conditions.

temporomandibular joint ankylosis associated with psoriasis and familial mediterranean fever a rare case report

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Temporomandibular Joint Ankylosis Associated with Psoriasis and Familial Mediterranean Fever: A Rare Case Report.”

eosinophilic granulomatosis with polyangiitisResearch

A large European cohort study identifies predictors of relapse and glucocorticoid dependence in eosinophilic granulomatosis with polyangiitis. These findings could inform treatment strategies and improve patient management.

prediction of relapse and glucocorticoid dependence in eosinophilic granulomatosis with polyangiitis findings from a large european cohort

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Prediction of Relapse and Glucocorticoid Dependence in Eosinophilic Granulomatosis with Polyangiitis: Findings from a Large European Cohort.”

tropical sprueResearch

A narrative review highlights tropical sprue as a neglected malabsorption syndrome, emphasizing the need for increased awareness and research. The review discusses its clinical features and potential treatment options.

tropical sprue a narrative review of a neglected malabsorption syndrome

PubMed Rare Disease·9 months ago·Read at source →

Original title: “Tropical sprue: a narrative review of a neglected malabsorption syndrome.”

Previous470 / 489Next

Daily Briefings

Not rare diseases news,news about your rare disease.

Earlier

A rare case study highlights the surgical and endovascular management of a mycotic common femoral artery pseudoaneurysm resulting from septic ankle arthritis. This case contributes to the understanding of complications arising from septic arthritis.

Recent research highlights the association of autoimmune encephalitis with anti-recoverin antibodies, providing insights into potential biomarkers for diagnosis. This discovery may enhance understanding and treatment strategies for affected patients.

A recent study highlights the diagnostic challenges posed by benign thyroid nodules that can mimic residual disease in patients with concurrent thyroid and gastric diffuse large B-cell lymphoma. The research emphasizes the importance of ultrasound-guided biopsy for accurate diagnosis.

A recent study evaluates the risks of dengue outbreaks on blood donation safety in Australia, extending beyond known outbreak areas. This research highlights the need for enhanced monitoring and safety protocols in blood donation practices.

A recent study highlights the prognostic significance of myelodysplasia-related gene mutations in patients with FLT3-ITD-mutated acute myeloid leukemia. This research could influence treatment strategies and patient management in this specific leukemia subtype.

New research highlights the development of user-defined peptide libraries that enhance the sensitive detection of cancer antigens. This advancement could improve diagnostic capabilities in oncology.

Recent research indicates that targeting the PD-1 pathway may reduce inflammation and fibrosis in systemic sclerosis. This discovery could lead to new therapeutic strategies for managing this challenging condition.

A case report details posterior reversible encephalopathy syndrome occurring with intracranial hemorrhage following split-liver transplantation. This finding contributes to the understanding of complications associated with liver transplants.

A recent publication explores the mechanisms and safety of statins in gastroenterology, highlighting human evidence supporting their use. This research may influence treatment strategies for gastrointestinal conditions.

A recent study explores multimodality imaging insights in a rare adult survivor of Taussig-Bing heart with pulmonary hypertension. This research contributes to understanding the complexities of this rare congenital heart defect.

A study published in PubMed examines bronchiectasis characteristics in patients with various genotypes of severe α(1)-antitrypsin deficiency. The findings contribute to understanding the disease's impact on lung health.

A novel protein truncating mutation in the TTC8 gene has been identified as the cause of Bardet-Biedl Syndrome in a Pakistani family. This discovery adds to the understanding of genetic factors contributing to BBS.

A multicenter study by the Korean Society of Spinal Tumors evaluates the feasibility and oncologic outcomes of en bloc resection with intentional tumor transgression in primary spinal sarcoma. This research contributes to understanding surgical approaches in treating this rare cancer.

A recent case study highlights the diagnostic challenges and surgical management of adenoid cystic carcinoma of the larynx. The findings emphasize the need for long-term surveillance in patients to monitor for recurrence.

A recent study highlights the dual pathology of fibrillary glomerulonephritis and apolipoprotein A-IV amyloidosis, diagnosed using mass spectrometry and DNAJB9 immunohistochemistry. This research contributes to the understanding of these rare diseases and their diagnostic challenges.

A recent publication discusses a case study of multiple oral white papules in a 3-year-old girl, prompting further investigation into potential underlying conditions. This case highlights the importance of clinical quizzes in diagnosing rare presentations in pediatric patients.

A recent study explores the clinical, surgical, and histopathological aspects of carpal tunnel syndrome in patients with mucopolysaccharidosis type I. The findings contribute to understanding the complications associated with this rare disease.

A rare case report highlights the association of temporomandibular joint ankylosis with psoriasis and familial Mediterranean fever. This finding may provide insights into the complex interplay between these conditions.

A large European cohort study identifies predictors of relapse and glucocorticoid dependence in eosinophilic granulomatosis with polyangiitis. These findings could inform treatment strategies and improve patient management.

A narrative review highlights tropical sprue as a neglected malabsorption syndrome, emphasizing the need for increased awareness and research. The review discusses its clinical features and potential treatment options.

Not rare diseases news,
news about your rare disease.