journal
https://read.qxmd.com/read/39252412/intramuscular-venous-malformation-associated-with-muscle-herniation-of-the-left-masseter-muscle-in-a-12-year-old-boy
#1
JOURNAL ARTICLE
Sultan Abdulwadoud Alshoabi, Saba'a Abdulmalik Amer, Abdulaziz A Qurashi, Fahad H Alhazmi, Eman Abdullah Al-Salami, Abdullgabbar M Hamid, Tareef S Daqqaq
BACKGROUND Muscle hernias are an uncommon condition typically found in the extremities; masseter muscle hernia is even rarer. However, it is important for clinicians and radiologists to be aware of this possibility. Intramuscular venous malformation (IMVM) is also uncommon and mostly found in the head, neck, and extremities. The simultaneous presence of both conditions is extraordinary uncommon, and, to our knowledge, this has not been reported before in the masseter muscle. Due to their rarity, vague presentation, and inaccurate clinical diagnosis, radiological evaluation is needed to avoid inappropriate surgical planning...
September 10, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39245905/dangers-of-herpesvirus-infection-in-sle-patients-under-anifrolumab-treatment-case-reports-and-clinical-implications
#2
JOURNAL ARTICLE
Mads Lamm Larsen, Morten Kelder Skouboe, Trine Hyrup Mogensen, Alex Lund Laursen, Bent Deleuran, Anne Troldborg, Mads Nyhuus Bendix Rasch
BACKGROUND Anifrolumab, a monoclonal antibody targeting the type 1 interferon (IFN-I) signaling pathway, holds promise as a therapeutic intervention for systemic lupus erythematosus (SLE). However, its use is associated with an increased risk of infections, particularly viral infections like herpes zoster (HZ). Results from the clinical trials on anifrolumab show yearly rates of upper respiratory tract infections of 34% and HZ of 6.1%. An increased frequency of other specific viral infections, including herpes simplex virus (HSV), was not reported...
September 9, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39244658/complex-presentation-of-pheochromocytoma-hypertensive-encephalopathy-and-takotsubo-like-cardiomyopathy-in-a-young-female
#3
JOURNAL ARTICLE
Nidhi Garg, Lekhya Raavi, Surabhi Maheshwari, Nafiye Busra Celik, Ashu Rastogi, Pankaj Garg
BACKGROUND Pheochromocytoma, a rare catecholamine-secreting tumor, often presents with paroxysmal or sustained hypertension, tachycardia, headache, and diaphoresis. Timely diagnosis is essential to prevent adverse complications. Less common presentations include pheochromocytoma crisis, with severe neurological and cardiac complications. CASE REPORT We report a unique case of a 25-year-old woman who initially presented with pheochromocytoma-induced hypertensive encephalopathy and acute coronary syndrome. Echocardiography revealed takotsubo-like cardiomyopathy, and magnetic resonance imaging of the brain revealed posterior reversible encephalopathy syndrome...
September 8, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39243128/unveiling-pheochromocytoma-a-puzzling-prelude-of-nausea-vomiting-and-abdominal-pain
#4
JOURNAL ARTICLE
Hannah R Klatzkow, Qi Cai, Ariel W Aday
BACKGROUND Pheochromocytomas, rare tumors arising from the adrenal medulla, can present with highly variable symptoms; therefore, pheochromocytomas frequently remain undiagnosed, leaving the potential for physiological complications. Acutely, these complications include pheochromocytoma crisis, in which high levels of catecholamines are released and cause a life-threatening hypertensive emergency. Over time, undiagnosed pheochromocytomas can lead to cardiovascular damage and end-organ disease related to chronic exposure to elevated blood pressure...
September 7, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39238181/pediatric-pyloric-transection-an-unusual-injury-following-blunt-abdominal-trauma
#5
JOURNAL ARTICLE
Saud Aljadaan, Rahaf Y Ardah, Raseel A Alsubaie, Suliaman Alaqeel
BACKGROUND The pediatric population, due to its distinct anatomy and physiology, often presents with unique mechanisms of trauma, leading clinicians to encounter diverse and sometimes unexpected injuries. Whether these injuries result from blunt or penetrating trauma, they may involve intra-abdominal organs in pediatric patients. Additionally, there are occasional occurrences where injuries affect rare sites such as the pylorus in an isolated manner within this age group. Clinicians must be prepared to address a wide range of injury patterns to ensure optimal outcomes for pediatric patients experiencing trauma to intra-abdominal structures such as the pylorus...
September 6, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39233392/hydrogel-based-dressings-and-multidisciplinary-care-in-severe-pediatric-burns-a-case-report-of-successful-healing-and-hypertrophic-scar-prevention
#6
JOURNAL ARTICLE
Yasser Ali Badereldien, Ghaleb Abdo Al-Mekhlafi
BACKGROUND Pediatric burn injuries are a global health concern, particularly in infants and toddlers, who face increased risks owing to their higher water content. Despite substantial medical treatment, the mortality rates remain challenging, especially in severe cases. This study explored non-surgical interventions for pediatric burn injuries, aiming to enhance care and alleviate the burden on affected children. CASE REPORT A 16-month-old boy with 30% mixed second- and third-degree burns presented with a scald injury...
September 5, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39228112/optimal-airway-management-in-severe-maxillofacial-trauma-a-case-report-on-submental-intubation
#7
JOURNAL ARTICLE
Ahmad Alsaka Amini, Abeer Alzuabi, Palna Kulkarni, Wala Sharif Ahmed, Mahmoud Salem Helal, Najah Albayedh, Amjad Zaaroura, Raneen Essale
BACKGROUND Submental intubation, a technique often considered a good alternative for managing the airway in challenging maxillofacial surgical scenarios, plays a pivotal role in providing accessibility to the surgical site and ensuring airway safety, particularly in cases involving facial fractures. This innovative approach not only grants surgeons adequate access to the operative field but also mitigates potential complications associated with traditional intubation methods, making it a valuable tool in dealing with complex facial trauma cases...
September 4, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39223781/rare-right-ventricular-calcified-amorphous-tumor-mimicking-malignancy-a-case-report
#8
JOURNAL ARTICLE
Ka Chun Lu, Cuixian Xie, Jie Chen, Zhongsheng Kuang, Rui Peng
BACKGROUND Cardiac calcified amorphous tumor (CCAT), a peculiar and uncommon non-neoplastic cardiac lesion, was initially characterized by Reynolds and colleagues in the medical literature in 1997. This distinctive entity is hallmarked by its unique feature of pedunculated and diffused calcifications, primarily infiltrating the cardiac structures, with a predilection for the mitral valve annulus initially, followed in sequence by the right atrium, right ventricle, left atrium, left ventricle, and tricuspid valve annulus...
September 3, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39219126/statin-induced-autoimmune-myopathy-a-diagnostic-challenge-in-muscle-weakness
#9
JOURNAL ARTICLE
Maryam Barkhordarian, Mark Grijalva, Albert Lee, Amer Jarri, Anna Belyayeva, Simcha Weissman
BACKGROUND Statin-induced myopathy can present with symptoms ranging from mild myalgia to significant muscle weakness. Muscle-related adverse effects of statins have been very challenging in clinical practice and they necessitate high clinical suspicion. This case report highlights how statin-induced autoimmune myopathy often goes undiagnosed. CASE REPORT We present a 69-year-old man with a past medical history of coronary artery disease who presented with myalgia and progressive proximal muscle weakness for 2 months, with a creatinine kinase of 8323 U/L...
September 2, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39217414/a-challenging-diagnosis-of-hhv-8-associated-diffuse-large-b-cell-lymphoma-not-otherwise-specified-in-a-young-man-with-newly-diagnosed-hiv
#10
JOURNAL ARTICLE
Ami Dave, Michael Schwartz, Jeremy Van, Laura Owczarzak, Ira Miller, Shivi Jain
BACKGROUND Human herpesvirus-8 (HHV-8)-associated diffuse large B-cell lymphoma, not otherwise specified (DLBCL, NOS), is a rare form of lymphoid malignancy. It poses unique challenges in diagnosis in the setting of human immunodeficiency virus (HIV) infection and concomitant multiorgan dysfunction. CASE REPORT We describe the case of a 26-year-old man who initially presented with pre-syncope and was found to have HIV, with a CD-4 count of 20 cells/μL. His initial clinical presentation was significant for nonspecific symptoms, isolated anemia, and bilateral pleural effusions without gross lymphadenopathy, which was initially attributed to acute HIV infection...
September 1, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39215452/chronic-myeloid-leukemia-with-a-rare-philadelphia-chromosome-variant-involving-chromosome-16
#11
JOURNAL ARTICLE
Salem M Bahashwan
BACKGROUND Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by the presence of the Philadelphia (Ph) chromosome, which results from the fusion of the translocation of the ABL1 gene from chromosome 9 to the BCR gene located in chromosome 22, forming the BCR-ABL gene on chromosome number 22, which accounts for approximately 95% of CML cases. Complex translocation involving other chromosomes can occur. CASE REPORT We present a rare case of CML with a variant Ph chromosome, in which chromosome 16 was involved with the usual translocation...
August 31, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39210578/concurrent-gitelman-syndrome-and-hyperthyroidism-diagnostic-challenges-in-a-51-year-old-patient
#12
JOURNAL ARTICLE
Yan Zhang, Hao Yu, Jun Li, Ling Cheng
BACKGROUND Gitelman syndrome (GS) is an uncommon autosomal recessive inherited disease caused by inactivating mutations in the SLC12A3 gene located on chromosome 16q13, resulting in distal tubular dysfunction. Most cases are detected during routine examinations in adulthood, due to hypokalemia and alkalosis. GS needs to be distinguished from diseases that cause hypokalemia, such as Classic Bartter syndrome and hyperthyroidism. In individual cases, GS and hyperthyroidism occur simultaneously, which is prone to misdiagnosis...
August 30, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39205369/adult-onset-pfapa-syndrome-successful-management-with-colchicine
#13
JOURNAL ARTICLE
Amulya Balagani, Farina Tariq, Muhammad Zaheer
BACKGROUND Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome is an autoinflammatory fever syndrome primarily seen in children under age 5 years, and its etiology is unknown. Most cases are resolved by the age of 10 years, and it is rare in adults. PFAPA is characterized by recurrent episodes of fever associated with pharyngitis, stomatitis, and cervical adenitis, although not all clinical features are present at initial evaluation. Diagnosis is made clinically, as there are no specific biomarkers available...
August 29, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39192560/malignant-pericardial-effusion-from-cervical-squamous-cell-carcinoma-a-case-study
#14
JOURNAL ARTICLE
Sunder Sham, Saroja Devi Geetha, Alae Kawam, Ahmed Bendari, Reham Al-Refai, F N U Anjali, Manju Harshan, Kasturi Das
BACKGROUND Cervical cancer ranks fourth globally among women's cancers. Squamous cell carcinoma constitutes 70% of cervical cancer cases, often metastasizing to lungs and paraaortic nodes. Uncommon sites include the brain, skin, spleen, and muscle, while pericardial fluid metastasis is highly rare. We report a case of squamous cell carcinoma of the uterine cervix that was metastatic to the pericardium and was detected on cytologic evaluation of pericardial fluid. CASE REPORT A 42-year-old woman who was previously treated for stage III squamous cell carcinoma of the cervix presented with symptoms of cough, fever, and shortness of breath for 8 days, and chest pain for 3 days...
August 28, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39188039/acute-neck-pain-from-crowned-dens-syndrome-a-case-report-and-clinical-insights
#15
JOURNAL ARTICLE
Lin Xie, Hanmo Fang, Chenpeng Dong, Min Cui, Kangcheng Zhao, Cao Yang, Xinghuo Wu
BACKGROUND Crowned dens syndrome (CDS) is a rare condition characterized by deposition of calcium pyrophosphate crystals on the odontoid process of the second cervical vertebra, forming a calcified 'crown', with neck pain being a common symptom. The disorder exhibits unique clinical and radiological features, resembling manifestations of meningitis, such as acute headaches and cervical stiffness. There are few case reports and case series related to CDS. Patients generally respond well to treatment with nonsteroidal anti-inflammatory drugs (NSAIDs), although there is a certain rate of recurrence...
August 27, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39183473/early-detection-of-subclinical-corneal-abnormalities-biophotonic-imaging-reveals-hyporeflective-bleb-like-structures-in-asymptomatic-eyes
#16
JOURNAL ARTICLE
Katharina Anna Sterenczak, Karsten Sperlich, Sebastian Bohn, Friederike Schaub, Oliver Stachs
BACKGROUND This case report illustrates the incidental detection of atypical hyporeflective bleb-like structures in an otherwise asymptomatic human cornea, highlighting the effectiveness of non-invasive biophotonic imaging techniques such as optical coherence tomography (OCT) and large-area confocal laser scanning microscopy (CLSM). CASE REPORT A 57-year-old man underwent a comprehensive ophthalmological examination, including slit-lamp biomicroscopy, corneal topography, and densitometry, as part of a clinical study...
August 26, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39182163/misdiagnosed-antibiotic-induced-liver-injury-unveiling-acute-hepatitis-e-in-a-65-year-old-patient
#17
JOURNAL ARTICLE
Sereina Livia Müller, Anna Kaumanns, Kai-Manuel Adam, Michael Osthoff, Sarah Dräger
BACKGROUND Common causes of severely elevated transaminases, especially alanine transaminase, due to liver diseases include drug-induced liver injury and acute viral hepatitis, especially hepatitis E, which can present similarly in clinical practice. Broad differential diagnostic workup in patients with elevated transaminases is required to not overlook the possibility of hepatitis E infection. CASE REPORT We report on a 65-year-old asymptomatic man who was referred to the Emergency Department from the rehabilitation center due to markedly elevated liver transaminases...
August 25, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39180199/bifidobacterium-bloodstream-infection-in-a-lymphoma-patient-undergoing-chemotherapy-a-case-study-and-implications-for-probiotic-use
#18
JOURNAL ARTICLE
Osamu Imataki, Makiko Uemura
BACKGROUND Fermenting bacilli producing lactic acid, including Bifidobacterium spp., are supposed to have low pathogenicity and no virulence for humans. Probiotics consisting of those fermenting bacilli can prevent and treat symptomatic gastrointestinal conditions, such as diarrhea. We use probiotics even in cancer patients, those who are immunocompromised, because a preferable effect to the intestinal commensal microbiome has been shown in a recent report. Some case reports warn of a rare risk of bloodstream infection caused by probiotics...
August 24, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39175175/challenges-in-diagnosing-metastatic-uterine-pecoma-insights-from-two-case-studies
#19
JOURNAL ARTICLE
Cédric Kabeya, Mathilde Lancelle, Gregory Demolin, Céline Wattier, Camille Marchisello, Antonino Buonomo, Sandhya Fonseca
BACKGROUND Perivascular epithelioid cell tumor (PEComa) is usually a benign perivascular tumor that expresses both melanocytic and myogenic cell markers. We report 2 cases of advanced malignant uterine perivascular epithelioid cell tumor (PEComa) in a 74-year-old woman and a 50-year-old woman undergoing surgery in our center. CASE REPORT Case 1: A 74-year-old woman presented with a painful and massive abdominal mass. The imaging revealed a 19-cm necrotic mass close to the mesentery, a suspicious lesion in the uterus, and a probable liver metastasis...
August 23, 2024: American Journal of Case Reports
https://read.qxmd.com/read/39169602/pigmented-villonodular-synovitis-of-the-shoulder-a-case-report-and-literature-review
#20
REVIEW
Vasileios Giannatos, Sosanna Ierodiaconou, Konstantinos Koutas, Evangelia Argyropoulou, Evangelos Sakellariou, Zinon T Kokkalis
BACKGROUND Pigmented villonodular synovitis is a rare clinical entity, with 2-3% of all PVNS cases affecting the shoulder. Diagnosis is challenging and can elude clinicians for years, with definitive treatment involving arthroscopic or open synovectomy. CASE REPORT A 50-year-old woman presented with left shoulder pain persisting for 2 years. She was initially conservatively treated by a rheumatologist, with corticosteroid schemes intra-articularly injected and per os, but no improvement of her symptoms was noted...
August 22, 2024: American Journal of Case Reports
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