keyword
https://read.qxmd.com/read/38706999/a-rare-case-of-severe-mitral-stenosis-presenting-as-cardiogenic-shock
#1
Lucas Garcia Reinoso, Sabu John
We report a case of severe mitral stenosis (MS) in a 58-year-old female from Guyana. Though rheumatic MS continues to be less prevalent in third-world countries, it poses a significant threat as far as morbidity and mortality are concerned. The modern definition of "Third World" is used to classify countries that are poor or developing. Countries that are part of the "third world" are generally characterized by (1) high rates of poverty, (2) economic and/or political instability, and (3) high mortality. The standard method of diagnosing MS in patients has been established as transthoracic echocardiograms (TTE), along with pertinent historical and physical exam findings...
April 2024: Curēus
https://read.qxmd.com/read/38428960/immune-checkpoint-inhibitor-associated-remitting-seronegative-symmetrical-synovitis-with-pitting-edema-description-of-a-new-entity-by-canrio
#2
JOURNAL ARTICLE
Azin Rouhi, Shahin Jamal, Lourdes Gonzales Arreola, David Moon, Marie Hudson, Janet Roberts, Alexandra Ladouceur, Carrie Ye
OBJECTIVE: Remitting seronegative symmetrical synovitis with pitting edema (RS3PE) is characterized by symmetrical synovitis with pitting edema and negative rheumatoid factor (RF). It has been described in a setting of malignancy, suggesting a paraneoplastic association. With the increasing use of immune checkpoint inhibitors (ICIs) for the treatment of cancers and emergence of immune-related adverse events (irAEs), our objective was to identify and describe cases of ICI-associated RS3PE (ICI-RS3PE) and compare them to non-ICI-RS3PE...
May 1, 2024: Journal of Rheumatology
https://read.qxmd.com/read/38414232/a-case-of-trauma-related-angioedema-of-the-airway-in-a-patient-on-an-angiotensin-receptor-blocker
#3
JOURNAL ARTICLE
Saint-Martin Allihien, Sammudeen Ibrahim, Swethapriya Chaparala, Shreyas Singireddy, Onoriode Kesiena
BACKGROUND Angioedema is non-pitting edema that occurs in the deep layers of the skin and subcutaneous tissue due to vascular leakage of plasma resulting from 1 of 2 major pathophysiological processes: mast cell-mediated angioedema and bradykinin-mediated angioedema. While it is a well-recognized adverse reaction of angiotensin-converting enzyme inhibitors, the association of angioedema with angiotensin receptor blockers is relatively less studied. Direct local trauma, although rarely, has been suggested to induce angioedema under certain conditions...
February 28, 2024: American Journal of Case Reports
https://read.qxmd.com/read/38350929/treatment-of-scleredema-adultorum-of-buschke-with-intravenous-immunoglobulin-and-mycophenolate-mofetil-in-a-14-year-old-girl-a-case-report
#4
JOURNAL ARTICLE
Mehran Pournazari, Dena Mohamadzadeh, Shirin Assar, Mazaher Ramezani
BACKGROUND: Scleredema adultorum of Buschke is a rare disease characterized by firm and non-pitting edema of the skin. The condition is rare with unknown etiology. Diagnosis is made on the basis of clinical findings and skin biopsy. CASE PRESENTATION: Here, we describe a 14-year-old Iranian girl presenting with non-pitting edema and woody thickening of the skin that progressed within a month. She was evaluated for possible underlying malignancy or connective tissue disorders, which were excluded by multiple laboratory workups...
February 14, 2024: Journal of Medical Case Reports
https://read.qxmd.com/read/38313922/injected-drug-addiction-associated-swollen-hands-a-case-report-of-methylamphetamine-related-unilateral-drug-addiction-related-puffy-hand-syndrome
#5
Philip R Cohen
Puffy hand syndrome occurs in addicts who have injected drugs either intravenously, intradermally, or subcutaneously. It usually presents as bilateral reversible pitting edema of the hands; less frequently, it occurs unilaterally. The forearms and arms may also be affected. The onset of puffy hand syndrome can occur while the patient is still injecting drugs; however, it can initially appear several years after injection of the drug has been discontinued. Infection with hepatitis C is a common comorbidity. A 47-year-old man is described who had a 20-year history of injecting methylamphetamine only into his non-dominant left arm, forearm, and hand and experienced his second episode of unilateral puffy hand syndrome four years after discontinuing injecting the drug and three years after his initial episode; he also had hepatitis C infection...
January 2024: Curēus
https://read.qxmd.com/read/38196481/a-case-of-stuck-mechanical-tricuspid-valve
#6
Abdul Nasir, Mujeeb Ur Rehman, Salman Khan, Hamza Ali
A 34-year-old non hypertensive, non-diabetic and ill looking weak woman came to our emergency department with shortness of breath NYHA III-IV, severe bilateral pedal edema extending up to the thighs and gross ascites. Physical examination revealed 3mm pitting ankle and leg edema and hemodynamically was stable with raised jugular venous pressure. There was a closing and opening mechanical click on Cardiac auscultation. At the lower left sternal border, there was grade 2/6 holodiastolic rumble and a grade 2/6 systolic murmur...
2024: Pakistan Journal of Medical Sciences Quarterly
https://read.qxmd.com/read/38130895/late-onset-melorheostosis-a-case-report
#7
Thanh Toan Vo, Kha To, Thanh Nghia Dang, Toan Phuc Vo, Duc Thien Nguyen, Duc Cong Nguyen, Manh Khanh Nguyen, Van Thai Nguyen
Melorheostosis is a rare benign bone pathology involving bone dysplasia and hyperostosis. The disease can be recognized with a characteristic radiographic feature of radiopaque lesions dripping along a long bone's diaphysis. The aberrant bone formation and development manifests mainly as pain, edema, and paresthesia of the affected limb. Severe cases may report limb deformity as well as limited range of motion. Until now, there have been approximately 300 cases reported about melorheostosis worldwide and its diverse clinical picture and age distribution...
2023: Case Reports in Oncology
https://read.qxmd.com/read/38107667/elephantiasis-nostras-verrucosa-a-treated-case-with-dietary-intervention-and-acitretin
#8
Laila Tsaqilah, Nadia Octavia, Risa Miliawati Nurul Hidayah, Erda Avriyanti, Hartati Purbo Dharmadji
Elephantiasis nostras verrucosa (ENV) is a rare and extreme complication of chronic non-filarial lymphedema. It can lead to severe disfiguration of body parts, especially the lower extremities, and is characterized by non-pitting edema and papulonodules with a verrucose or cobblestone-like appearance. Obesity is a risk factor of ENV. Various treatments have been reported for ENV. A 52-year-old woman presented to our outpatient dermatology clinic with non-pitting edema, cobblestone-like papulonodules, and erythematous plaques on both legs for 2 years...
2023: Clinical, Cosmetic and Investigational Dermatology
https://read.qxmd.com/read/38102695/elephantiasis-mimicry-in-recurrent-lower-limb-skin-infections-in-a-diabetic-patient-a-case-report
#9
JOURNAL ARTICLE
Puneet Bramania, Emmaeli Moshi, Andrew Foi, Grace Shayo
BACKGROUND: Chronic edema as a complication of systemic diseases or infections can mimic filarial lymphedema (also known as elephantiasis) and considered so. We describe a case of chronic lymphedema that mimicked elephantiasis in a diabetic man. CASE PRESENTATION: The patient was a 70-year-old black man, bed-bound at the time of admission following a diagnosis of stroke and hypertension in the previous 5 years. He had been diabetic for 20 years with poorly controlled diabetes mellitus...
December 16, 2023: Journal of Medical Case Reports
https://read.qxmd.com/read/38060742/systemic-lupus-erythematosus-flare-masquerading-as-bilateral-lower-extremity-non-pitting-edema-a-case-report
#10
Ayesha Khan, Hala Mouhydeen, Hussein Gharib
Systemic lupus erythematosus (SLE) is a complex autoimmune disease that affects multiple organ systems in the body. We report the case of a patient with new-onset bilateral lower extremity (LE) non-pitting edema as the only presenting symptom of a severe SLE flare. Other potential etiologies of non-pitting LE edema in patients with SLE were excluded, including hypothyroidism and lymphedema. Laboratory investigations and SLE disease activity index (SLEDAI) score suggested severe SLE flare. The edema improved with steroids and diuresis...
November 2023: Curēus
https://read.qxmd.com/read/38016521/peripapillary-fluid-obvious-and-not-so-obvious
#11
REVIEW
Supriya Arora, Dinah Zur, Claudio Iovino, Jay Chhablani
Intraretinal or subretinal fluid in the peripapillary area can be clinically visualized in conditions such as peripapillary choroidal neovascularization, optic disc pit maculopathy, and optic nerve head tumors and granulomas. Optical coherence tomography (OCT) helps to visualize peripapillary fluid in many other chorioretinal conditions such as peripapillary pachychoroid syndrome, posterior uveitis, central retinal vein occlusion, malignant hypertension, hypotonic maculopathy as well as neuro-ophthalmological conditions such as glaucoma, microcystic macular edema and disc edema due papilledema, non-arteritic anterior ischemic optic neuropathy, neuroretinitis, and diabetic papillopathy...
2024: Survey of Ophthalmology
https://read.qxmd.com/read/37960726/intralymphatic-histiocytosis-of-the-upper-eyelid-in-a-patient-of-korean-descent-a-case-report
#12
JOURNAL ARTICLE
Dong Hee Ha, Hee Sung Kim, Jeong Kyu Lee
RATIONALE: Diagnosing intralymphatic histiocytosis can be challenging due to its rarity. We present a case of intralymphatic histiocytosis in the upper eyelid of a Korean patient. We treated the condition by surgical debulking and intralesional triamcinolone injection. PATIENT CONCERNS: A 59-year-old man was referred to our clinic with a 7-year history of unilateral swelling in the right upper eyelid. He had previously been treated with long-term oral steroids and immunosuppressants, but his eyelid swelling persisted...
November 10, 2023: Medicine (Baltimore)
https://read.qxmd.com/read/37893596/elderly-onset-rheumatoid-arthritis-characteristics-and-treatment-options
#13
REVIEW
Slavica Pavlov-Dolijanovic, Milan Bogojevic, Tatjana Nozica-Radulovic, Goran Radunovic, Natasa Mujovic
Elderly-onset rheumatoid arthritis (EORA) is a distinct clinical entity defined as the onset of rheumatoid arthritis (RA) in individuals aged over 60 years. EORA presents unique clinical features, including a more equitable distribution of sexes, a potential predilection for male involvement, a higher incidence of acute onset characterized by constitutional symptoms, a propensity for systemic manifestations, elevated sedimentation rates at disease onset, a reduced occurrence of rheumatoid factor positivity, increased titers of anti-citrullinated protein antibodies, a preference for involvement of large joints, elevated disease activity, the presence of bone erosions, and heightened patient disability...
October 23, 2023: Medicina
https://read.qxmd.com/read/37835014/objective-methods-of-assessing-fluid-status-to-optimize-volume-management-in-kidney-disease-and-hypertension-the-importance-of-ultrasound
#14
REVIEW
Sharad Patel, Adam Green, Sandhya Ashokumar, Andrew Hoke, Jean-Sebastien Rachoin
Fluid overload, a prevalent complication in patients with renal disease and hypertension, significantly impacts patient morbidity and mortality. The daily clinical challenges that clinicians face include how to identify fluid overload early enough in the course of the disease to prevent adverse outcomes and to guide and potentially reduce the intensity of the diuresis. Traditional methods for evaluating fluid status, such as pitting edema, pulmonary crackles, or chest radiography primarily assess extracellular fluid and do not accurately reflect intravascular volume status or venous congestion...
October 5, 2023: Journal of Clinical Medicine
https://read.qxmd.com/read/37772217/diffuse-large-b-cell-lymphoma-mimicking-pancreatic-carcinoma-and-the-use-of-immunohistochemistry-in-resolving-the-diagnostic-dilemma-after-postmortem-examination-a-case-report
#15
Ifeanyichukwu D Nwanji, Babatope L Awosusi, Alexander O Odigwe, Mustapha A Ajani
Diffuse large B-cell lymphoma is the most common lymphoma, accounting for 30% of all non-Hodgkin lymphomas; they can grow rapidly and often present as masses infiltrating tissues or obstructing organs. We report the case of a 58-year-old female who presented with a one-month history of generalized body weakness and weight loss with a two-week history of yellowness of the eyes, fever, dyspnea, and bilateral leg swelling. Examination at presentation revealed pallor, fever, jaundice, hepatomegaly, and bilateral pitting pedal edema...
August 2023: Curēus
https://read.qxmd.com/read/37404402/a-delicate-balance-challenges-in-the-management-of-primary-hyperparathyroidism-and-congestive-heart-failure
#16
Nikita Mohan, Rupinder K Bahniwal, Manasi S Shah
Primary hyperparathyroidism (PHPT) is an excessive parathyroid hormone (PTH) production disorder, causing increased calcium levels. Commonly, these cases are asymptomatic and detected incidentally on routine labs. These patients are usually conservatively managed and monitored periodically, including bone and kidney health evaluation. Medical management of severe hypercalcemia secondary to PHPT includes IV fluids, cinacalcet, bisphosphonates, and dialysis, while the surgical treatment is parathyroidectomy. Patients suffering from heart failure with reduced ejection fraction (HFrEF) on diuretics and PHPT require a delicate balance of their volume status to prevent exacerbation of either condition...
June 2023: Curēus
https://read.qxmd.com/read/37271192/macular-retinoschisis-from-optic-disc-without-a-visible-optic-pit-or-advanced-glaucomatous-cupping-no-optic-pit-retinoschisis-nopir
#17
JOURNAL ARTICLE
Satoko Fujimoto, Gregg T Kokame, Edwin H Ryan, Mark W Johnson, Akito Hirakata, Ashley Shirriff, Hiroshi Ishikawa, Olufemi E Adams, Nikhil Bommakanti
PURPOSE: To review eyes with peripapillary and macular retinoschisis without a visible optic pit or advanced glaucomatous optic atrophy, or NOPIR (No Optic Pit Retinoschisis) DESIGN: Retrospective multi-center case series SUBJECTS: The study included 11 eyes of eleven patients. METHODS: Retrospective study of eyes with macular retinoschisis without a visible optic pit, advanced optic nerve head cupping, or macular leakage on fluorescein angiography. MAIN OUTCOME MEASURES: Visual acuity (VA), retinoschisis resolution, months to resolution, recurrence of retinoschisis RESULTS: Mean age was 68...
June 2, 2023: Ophthalmology Retina
https://read.qxmd.com/read/37193805/in-vivo-imaging-of-acute-physiological-responses-after-treatment-of-cancer-with-near-infrared-photoimmunotherapy
#18
JOURNAL ARTICLE
Kohei Nakajima, Akiyo Sugikawa, Hironobu Yasui, Kei Higashikawa, Chie Suzuki, Takahiro Natsume, Motofumi Suzuki, Hideo Takakura, Mayu Tomita, Sachi Takahashi, Kenji Hirata, Yasuhiro Magata, Yuji Kuge, Mikako Ogawa
PURPOSE: Near-infrared photoimmunotherapy (NIR-PIT) is a new cancer phototherapy using an antibody-photosensitizer conjugate (Ab-IR700). By NIR light irradiation, Ab-IR700 forms a water-insoluble aggregation on the plasma membrane of cancer cells, leading to lethal membrane damage of cancer cells with high selectivity. However, IR700 produces singlet oxygen, which induces non-selective inflammatory responses such as edema in normal tissues around the tumor. Understanding such treatment-emergent responses is important to minimize side effects and improve clinical outcomes...
May 16, 2023: Molecular Imaging and Biology: MIB: the Official Publication of the Academy of Molecular Imaging
https://read.qxmd.com/read/37124179/mannose-phosphate-isomerase-gene-mutation-leads-to-a-congenital-disorder-of-glycosylation-a-rare-case-report-and-literature-review
#19
REVIEW
Siliang Lu, Shuheng Liang, Yi Wu, Jinyi Liu, Lin Lin, Guosheng Huang, Huaijun Ning
We report the case of a 2-year-old girl who was diagnosed with Mannose-6-phosphate isomerase-congenital disorder of glycosylation (MPI-CDG) and provide a review of the relevant literature. The young girl presented with recurrent unexplained diarrhea, vomiting, hypoproteinemia, and elevated liver transaminases. Whole-exome sequencing revealed that the patient had compound heterozygous mutations in the MPI gene (NM_0024). An exon 4 (c.455G > T, p.R152l) mutation was inherited from the mother and an exon 7 (c...
2023: Frontiers in Pediatrics
https://read.qxmd.com/read/37062777/clinical-and-histological-features-and-treatment-outcomes-of-patients-with-morbihan-disease-a-systematic-review
#20
JOURNAL ARTICLE
Omkar Mayur, Rebeca Martinez, Megan C McNichol, Jean S McGee
Morbihan disease (MD) is considered a rare complication of rosacea, which is difficult to diagnose and challenging to treat. Here, we performed a systematic review of available case reports and case series to summarize key clinical and pathologic features of and successful treatment regimens for MD. We conducted a search of the PubMed/MEDLINE, EMBASE, and Cochrane electronic databases from their inception to the date of search on March 6, 2023. We found that MD affects patients in the fifth decade of life on average, more commonly reported in male than female (69% vs 31%)...
April 16, 2023: Archives of Dermatological Research
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