keyword
https://read.qxmd.com/read/38576992/paraneoplastic-pemphigus-in-a-patient-with-t-cell-lymphoma-a-case-report
#21
Yohannis Derbew Molla, Isak Omer Answar, Biruk Mulat Worku, Amanuel Kassa Tadesse, Elias Manaye Tefera, Bewketu Abebe Alemu, Gebrehiwot Lema Legese, Samuel Addisu Abera
INTRODUCTION AND IMPORTANCE: Paraneoplastic pemphigus (PNP) is an uncommon autoimmune mucocutaneous disease characterized by severe stomatitis, polymorphous skin eruptions, and the presence of underlying neoplasms. Unique histopathological features include suprabasal acantholysis and clefts with scattered necrotic keratinocytes. CASE PRESENTATION: A 27-year-old female patient presented with a 3-month history of a painless swelling, approximately the size of a pea, on the left lateral aspect of her neck and axillary area...
April 2024: Annals of Medicine and Surgery
https://read.qxmd.com/read/38576642/congenital-erythropoietic-porphyria-a-rare-inherited-disorder
#22
Porika Saikrishna, Gowrishankar Palaniswamy, Navya Pillikunte Doddareddy, Lyluma Ishfaq, Mah N Zargar, Fathima Wafa Eranhikkal, Sweta Sahu
Congenital erythropoietic porphyria (CEP), also known as Gunther's disease, is an uncommon autosomal recessive disorder caused by a mutation in the uroporphyrinogen III synthase gene. This mutation results in reduced enzyme levels in heme synthesis and the accumulation of pathogenic porphyrin isomers, uroporphyrin I and coproporphyrin I, leading to the clinical manifestations of CEP. Typically, CEP manifests shortly after birth with severe cutaneous photosensitivity, blistering, ulceration, and scarring. Erythrodontia, acro-osteolysis, and skeletal abnormalities are frequently present in conjunction with it...
March 2024: Curēus
https://read.qxmd.com/read/38576167/guillain-barre-syndrome-mimicking-brain-death
#23
JOURNAL ARTICLE
Mukesh Kumar Sarna, Sarthak Shah, Puneet Rijhwani, Gourav Goyal, Anand Kumar Jain, Pallaavi Goel
A 49-year-old female patient presented at the hospital with a history of herpetic blisters, frequent episodes of vomiting and loose stools, bilateral upper and lower limb weakness, and diminishing sensorium. She was diagnosed with hyponatraemia and respiratory failure and later became unconscious with absent brainstem reflexes. The patient was initially treated for herpetic encephalitis, a chronic obstructive pulmonary disease with acute exacerbation, hyponatraemia and neuroparalytic snake bite. Further evaluation, however, identified the uncommon Guillain Barre syndrome presentation with overlap of Bickerstaff brainstem encephalitis...
April 4, 2024: Journal of the Royal College of Physicians of Edinburgh
https://read.qxmd.com/read/38575929/alternatives-to-dental-opioid-prescribing-after-tooth-extraction-adopt-protocol-for-a-stepped-wedge-cluster-randomized-trial
#24
JOURNAL ARTICLE
Douglas R Oyler, Philip M Westgate, Sharon L Walsh, Jennifer Dolly Prothro, Craig S Miller, Monica F Roberts, Patricia R Freeman, Hannah K Knudsen, Maggie Lang, Enif Dominguez-Fernandez, Marcia V Rojas-Ramirez
BACKGROUND: Dentists and oral surgeons are leading prescribers of opioids to adolescents and young adults (AYA), who are at high risk for developing problematic opioid use after an initial exposure. Most opioids are prescribed after tooth extraction, but non-opioid analgesics provide similar analgesia and are recommended by multiple professional organizations. METHODS: This multi-site stepped wedge cluster-randomized trial will assess whether a multicomponent behavioral intervention can influence opioid prescribing behavior among dentists and oral surgeons compared to usual practice...
April 4, 2024: BMC Oral Health
https://read.qxmd.com/read/38575061/flow-diverter-combined-with-coil-embolization-for-acutely-ruptured-intracranial-aneurysms-a-single-center-experience
#25
JOURNAL ARTICLE
Jie Liu, Liyun Zhou, Yuhui Ling, Xiuzhi Xiang, Peiming Wang
BACKGROUND AND PURPOSE: Extensive research has confirmed the safety and effectiveness of flow diverters in the treatment of unruptured intracranial aneurysms. However, their use in cases of acute rupture remains a subject of debate. METHODS: This study was conducted as a single-center retrospective investigation from January 2018 to January 2022 and included patients with acutely ruptured intracranial aneurysms (within three days of rupture) who were treated using the Pipeline Embolization Device (PED) with adjunctive coil embolization...
April 2, 2024: World Neurosurgery
https://read.qxmd.com/read/38569886/safety-and-efficacy-of-coated-flow-diverters-in-the-treatment-of-ruptured-intracranial-aneurysms-a-retrospective-multicenter-study
#26
JOURNAL ARTICLE
Lukas Goertz, Sophia Hohenstatt, Dominik F Vollherbst, Charlotte Sabine Weyland, Omid Nikoubashman, Hanna Styczen, Christian Gronemann, Daniel Weiss, Marius Kaschner, Muriel Pflaeging, Eberhard Siebert, David Zopfs, Jonathan Kottlors, Lenhard Pennig, Marc Schlamann, Georg Bohner, Thomas Liebig, Bernd Turowski, Franziska Dorn, Cornelius Deuschl, Martin Wiesmann, Markus A Möhlenbruch, Christoph Kabbasch
BACKGROUND: This multicenter study evaluated the safety and efficacy of coated flow diverters (cFDs) for the treatment of ruptured intracranial aneurysms. METHODS: Consecutive patients treated with different cFDs for ruptured aneurysms under tirofiban at eight neurovascular centers between 2016 and 2023 were retrospectively analyzed. The majority of patients were loaded with dual antiplatelet therapy after the treatment. Aneurysm occlusion was determined using the O'Kelly-Marotta (OKM) grading scale...
April 3, 2024: Journal of Neurointerventional Surgery
https://read.qxmd.com/read/38566380/skin-microbial-composition-and-genetic-mutation-analysis-in-precision-medicine-for-epidermolysis-bullosa
#27
JOURNAL ARTICLE
Inna Syafarina, Maulida Mazaya, Ariani Indrawati, Sharfina Zahra Akbar, Rifki Sadikin, Caecilia Sukowati
Epidermolysis bullosa (EB) is an inherited skin disease representing a spectrum of rare genetic disorders. These conditions share the common trait that causes fragile skin, resulting in the development of blisters and erosions. The inheritance follows an autosomal pattern, and the array of clinical presentations leads to significant physical suffering, considerable morbidity, and mortality. Despite EB having no cure, effectively managing EB remains an exceptional challenge due to its rarity and complexity, occasionally casting a profound impact on the lives of affected individuals...
April 1, 2024: Current Drug Targets
https://read.qxmd.com/read/38563276/glastonbury-festival-medical-care-at-the-world-s-largest-greenfield-music-festival
#28
JOURNAL ARTICLE
Jack F Bennett, David J Cottrell
INTRODUCTION: Music festivals have become an increasingly popular form of mass-gathering event, drawing an increasing number of attendees across the world each year. While festivals exist to provide guests with an enjoyable experience, there have been instances of serious illness, injury, and in some cases death. Large crowds, prolonged exposure to loud music, and high rates of drug and alcohol consumption can pose a dangerous environment for guests as well as those looking after them...
April 2, 2024: Prehospital and Disaster Medicine
https://read.qxmd.com/read/38559535/to-debride-or-not-to-debride-a-review-of-wound-management-for-stevens-johnson-syndrome-and-toxic-epidermal-necrolysis
#29
REVIEW
Christina D Enescu, Adam J Elder, Hany Deirawan, Meena Moossavi
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are immune-mediated skin reactions with high mortality as a result of severely compromised skin barrier function. Currently, there is no consensus on the topical management of these conditions. Some advocate for surgical debridement of affected skin as a means of preventing infection and facilitating reepithelialization with synthetic and biological wound coverage. Others prefer a conservative approach that relies on leaving the blistered skin in situ...
March 2024: Curēus
https://read.qxmd.com/read/38558580/physiotherapeutic-interventions-in-diabetic-foot-ulcer-management-a-case-report
#30
Vaishnavi R Waghe, Vrushali Athawale
Diabetic foot ulcers (DFUs) represent prominent complications arising from diabetes mellitus, characterized by the development of severe and persistent wounds involving the loss of epidermal and/or dermal layers, with the potential to extend into subcutaneous and underlying tissue structures. In the presented case, a 62-year-old male patient presented with complaints of pain and the emergence of blisters on the right foot, marked by an insidious onset and gradual progression in size, ultimately leading to ulcer formation subsequent to blister rupture...
February 2024: Curēus
https://read.qxmd.com/read/38558462/bone-marrow-transplantation-and-bone-marrow-derived-mesenchymal-stem-cell-therapy-in-epidermolysis-bullosa-a-systematic-review
#31
REVIEW
Maulidina Agustin, Anita Mahadewi, Retno Danarti
Epidermolysis bullosa (EB) is a genodermatosis that lacks effective treatments and requires supportive care for its severe, life-threatening manifestations. Bone marrow transplantation (BMT) and its derived cells have been suggested to improve clinical symptoms and quality of life. A comprehensive search was conducted for publications evaluating BMT and bone marrow-derived mesenchymal stem cell (BM-MSC) therapy for EB in PubMed/MEDLINE, Google Scholar, and Cochrane databases from inception until June 2023. A total of 55 participants with severe forms of EB had BMT and/or BM-MSCs, with recessive dystrophic EB as the most common EB type; 53 (96...
April 1, 2024: Pediatric Dermatology
https://read.qxmd.com/read/38557472/subepidermal-blistering-disease-presenting-with-anti-p200-and-anti-type-vii-collagen-autoantibodies
#32
JOURNAL ARTICLE
Anna Koshida, Chihiro Nishijima, Hiroshi Koga, Norito Ishii, Makoto Inaoki
No abstract text is available yet for this article.
February 1, 2024: European Journal of Dermatology: EJD
https://read.qxmd.com/read/38556206/-not-available
#33
R de Moraes Souza, T Bellón, E Fiz Benito, E Sendagorta Cudós
No abstract text is available yet for this article.
March 29, 2024: Actas Dermo-sifiliográficas
https://read.qxmd.com/read/38555437/post-radiation-lichen-planus-a%C3%A2-case-report-and-review-of-the-literature
#34
JOURNAL ARTICLE
Adam N Musick, Do Young Kim, Steven J Baumrucker
BACKGROUND: Lichen planus is a T-cell mediated inflammatory disorder of the skin and mucus membranes and is a rare complication of external beam radiation. CASE PRESENTATION: 64 year old White male who presented to dermatology with a lesion at the lateral aspect of the right thigh. The lesion was first noted 40 years prior and had grown from 1.5 cm to 6.5 cm in the ensuing years. On examination the lesion was raised, hypopigmented, with pearly borders and central ulceration...
March 31, 2024: Journal of Medical Case Reports
https://read.qxmd.com/read/38548397/-clinical-characteristics-of-11-patients-with-vibrio-vulnificus-infection-and-the-establishment-of-a-rapid-diagnosis-procedure-for-this-disease
#35
JOURNAL ARTICLE
W P Lin, X Mu, S H Chen, C J He, H H Li, C W Sun, H N Bian, W Lai, Z F Huang
Objective: To analyze the clinical characteristics of patients with Vibrio vulnificus infection, share diagnosis and treatment experience, and establish a rapid diagnosis procedure for this disease. Methods: This study was a retrospective case series study. From January 2009 to November 2022, 11 patients with Vibrio vulnificus infection who met the inclusion criteria were admitted to the Department of Burns and Wound Repair of Guangdong Provincial People's Hospital Affiliated to Southern Medical University...
March 20, 2024: Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi
https://read.qxmd.com/read/38546109/steven-jonhson-syndrome-in-a-patient-with-dengue-infection-in-peru-a-case-report
#36
JOURNAL ARTICLE
Winny D Aparcana-Choque, Yadira M Pisconti-Palacios, Ivan Cordova-Tello, Jhon Ausejo-Galarza, Walter Gomez-Gonzales, Andrei Kochubei-Hurtado, Kovy Arteaga-Livias
Stevens-Johnson syndrome is an infrequent condition affecting the skin and mucous membranes, it involves cutaneous detachment with high mortality without adequate treatment. We present the case of a 40-year-old male with a history of epilepsy treated with valproic acid and lamotrigine, previously diagnosed with dengue. Evaluation showed erythematous blisters on skin and mucosa with bleeding and desquamation, covering 10% of the body surface. The patient progressed favorably with the medical care received. Stevens-Johnson syndrome should be studied in association with arboviral diseases...
2024: Journal of Investigative Medicine High Impact Case Reports
https://read.qxmd.com/read/38544595/multidisciplinary-exploration-of-unknown-oral-lesions-with-accompanying-oral-verrucas-of-the-tongue-a-case-report
#37
Nafiz Khan, Navjot Dhoat, Ali Z Ansari, Joshua J Gallagher, Srihita Patibandla, Kurt Bruckmeier
A 64-year-old African American male with a history of hypertension and type II diabetes mellitus presented with unexplained upper lip lacerations after several frequent episodes of hemoptysis. Following the upper lip lacerations were several weeks of intermittent unknown episodic fevers. The patient, challenged by impaired mobility, exhibited an array of symptoms, including severe upper lip pain with lacerations and white patches on the tongue. Laboratory findings indicated thrombocytopenia and anemia, with positive tests for both influenza A and B...
February 2024: Curēus
https://read.qxmd.com/read/38537929/single-cell-profiling-unveils-the-inflammatory-heterogeneity-within-cutaneous-lesions-of-bullous-pemphigoid
#38
JOURNAL ARTICLE
Yue Ruan, Chuqiao Xu, Tianyu Zhang, Lin Zhu, Hailun Wang, Jingying Wang, Haiqin Zhu, Chuanxin Huang, Meng Pan
Bullous pemphigoid (BP) is a subepidermal blistering skin disease with a complex pathogenesis involving various immune cells. However, the transcriptional features of these cells remain poorly defined. Here, we construct a comprehensive and single-cell resolution atlas of various immune cells within BP skin lesions via integrative single-cell analysis, flow cytometry and multiplex immunohistochemistry. We observed prominent expansion and transcriptional changes in mast cells, macrophages, basophils, and neutrophils within BP lesions...
March 25, 2024: Journal of Investigative Dermatology
https://read.qxmd.com/read/38534263/claudin-4-upregulation-in-acantholytic-and-autoimmune-mediated-bullous-disorders
#39
JOURNAL ARTICLE
Chau M Bui, Huy G Vuong, Minh-Khang Le, Kristin J Rybski, Hatice B Zengin, Haiming Tang, Bruce R Smoller
Claudin-4 is a key component of tight junctions, which play an important role in the formation of the epidermal barrier by forming a circumferential network in the granular layer that serves as a gatekeeper of the paracellular pathway. The aim of this study is to illustrate claudin-4 immunohistochemical staining patterns of different blistering disorders. We collected 35 cases, including two Hailey-Hailey disease, one Darier disease, three Grover disease, one acantholytic acanthoma, two warty dyskeratoma, 11 pemphigus vulgaris (PV) including six mucosal PV, and two pemphigus foliaceus...
December 21, 2023: Dermatopathology (Basel, Switzerland)
https://read.qxmd.com/read/38526344/a-genome-sequence-for-the-threatened-whitebark-pine
#40
JOURNAL ARTICLE
David B Neale, Aleksey V Zimin, Amy Meltzer, Akriti Bhattarai, Maurice Amee, Laura Figueroa Corona, Brian J Allen, Daniela Puiu, Jessica Wright, Amanda R De La Torre, Patrick E McGuire, Winston Timp, Steven L Salzberg, Jill L Wegrzyn
Whitebark pine (WBP, Pinus albicaulis) is a white pine of subalpine regions in western contiguous US and Canada. WBP has become critically threatened throughout a significant part of its natural range due to mortality from the introduced fungal pathogen white pine blister rust (WPBR, Cronartium ribicola) and additional threats from mountain pine beetle (Dendroctonus ponderosae), wildfire, and maladaptation due to changing climate. Vast acreages of WBP have suffered nearly complete mortality. Genomic technologies can contribute to a faster, more cost-effective approach to the traditional practices of identifying disease-resistant, climate-adapted seed sources for restoration...
March 25, 2024: G3: Genes—Genomes—Genetics
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