keyword
MENU ▼
Read by QxMD icon Read
search

Visceral angioedema

keyword
https://www.readbyqxmd.com/read/26436796/-cutaneous-loxoscelism-mainly-edematous-a-case-report
#1
Paula de la Barra, Verónica Vial, Yenis Labraña, Ana María Álvarez, Helena Seguel
In Chile, loxoscelism is caused by the bite of the Loxosceles laeta spider. The clinical presentation has two different forms: cutaneous loxoscelism (CL) and vicero-cutaneous loxoscelism, which is less frequent. Cutaneous loxoscelism includes an uncommon clinical variation (4%), called CL with edematous predominance (CLEP). We present a 5-year-old patient with sudden pain and edema on his right eyelid associated with fever, which progressed rapidly involving the right hemifacial area, frontal region, and left eyelid...
August 2015: Revista Chilena de Infectología: órgano Oficial de la Sociedad Chilena de Infectología
https://www.readbyqxmd.com/read/25578409/visceral-angioedema-an-under-recognized-complication-of-angiotensin-converting-enzyme-inhibitors
#2
Sangeeta Mutnuri, Adnan Khan, Easwaran P Variyam
Cough and upper airway angioedema are well-recognized adverse reactions of angiotensin-converting enzyme inhibitor (ACEI) therapy. Visceral angioedema is an infrequent and often unrecognized complication of ACEI therapy. We describe a patient in whom the diagnosis was delayed for > 2 years. A 60-year-old woman with hypertension on treatment with enalapril presented with complaints of abdominal pain and diarrhea for 2 days. Physical examination was significant for diffuse abdominal tenderness and hypotension...
March 2015: Postgraduate Medicine
https://www.readbyqxmd.com/read/25317271/drug-induced-visceral-angioedema
#3
REVIEW
Prashanth M Thalanayar, Ibrahim Ghobrial, Fritz Lubin, Reena Karnik, Robin Bhasin
Angioedema associated with angiotensin converting enzyme inhibitors (ACEIs) is due to the accumulation of bradykinin and its metabolites. Angiotensin receptor blockers (ARBs) produce anti-hypertensive effects by blocking the angiotensin II AT1 receptor action; hence bradykinin-related side effects are not expected. However, we notice the occurrence of ARB-induced angioedema as not a very rare side effect. Visceral drug-induced angioedema has been reported with ACEIs, not with ARBs. This underlying review will help educate readers on the pathophysiology and recent guidelines pertaining to ACEI- and ARB-induced visceral angioedema...
2014: Journal of Community Hospital Internal Medicine Perspectives
https://www.readbyqxmd.com/read/25154179/-guidelines-for-the-diagnosis-and-treatment-of-hereditary-angioedema
#4
Asja Stipić Marković, Vojko Rozmanić, Branimir Anić, Neda Aberle, Goran Racić, Srdan Novak, Davor Sunara, Boris Grdinić, Ljerka Karadza-Lapić, Melanija Razov Radas, Boris Karanović, Barbara Kvenić
Hereditary angioedema (HAE) is a rare but potentially fatal genetic disorder with nonpitting, nonerythematous, and not pruritic swelling which can affect the hands, feet, face, genitals and visceral mucosa. The type, frequency, and severity of the attacks vary between patients, and over the lifetime of an individual patient. Efforts in Croatian counties have identified approximately 100 patients (but there must be more undiagnosed patients). The first global guideline for the management of HAE was developed by the World Allergy Organization HAE International Alliance and published in 2012...
May 2014: Lijec̆nic̆ki Vjesnik
https://www.readbyqxmd.com/read/25139411/immediate-hypersensitivity-reaction-following-liposomal-amphotericin-b-ambisome-infusion
#5
Proggananda Nath, Ariful Basher, Michiyo Harada, Santana Sarkar, Shahjada Selim, Richard J Maude, Eisei Noiri, Abul Faiz
Liposomal amphotericin-B (AmBisome) is now becoming first choice for the treatment of visceral leishmaniasis (kala-azar) patients due to high efficacy and less toxicity. The reported incidence of hypersensitivity reactions to liposomal amphotericin-B (AmBisome), especially during therapy, is very rare. We report two patients with kala-azar: one developed breathing difficulties and hypotension followed by shock and the other had facial angioedema with chest tightness during treatment. Both patients were managed with immediate action of injection: adrenaline, diphenhydramine and hydrocortisone...
October 2014: Tropical Doctor
https://www.readbyqxmd.com/read/24792779/radiologic-manifestations-of-angioedema
#6
Kousei Ishigami, Sarah L Averill, Janet H Pollard, Joshua M McDonald, Yutaka Sato
OBJECTIVES: The purpose of this pictorial review is to present imaging findings of angioedema involving the various organs. CONCLUSION: The role of imaging for patients with angioedema includes the evaluation of the upper airway for obstruction and the exclusion of other possible aetiologies, such as neoplastic or infectious processes. Glossomegaly is a common finding of head and neck angioedema. Angioedema may involve organ systems beyond the superficial regions and the head and neck including the gastrointestinal and genitourinary tracts...
June 2014: Insights Into Imaging
https://www.readbyqxmd.com/read/23878294/ace-inhibitor-induced-intestinal-angio-oedema-rare-adverse-effect-of-a-common-drug
#7
Lokesh Shahani
ACE inhibitors are the leading cause of drug-induced angio-oedema in the USA. ACE inhibitor-induced intestinal angio-oedema, a much rarer complication of this medication, has been reported. The author reports a patient presenting with a 1-day history of severe abdominal pain. The patient was started on lisinopril 2 days prior to this presentation. Computer axial tomography (CAT) scan of the abdomen demonstrated extensive and marked thickening, and oedema involving the duodenum and proximal jejunum associated with significant mesenteric oedema...
July 22, 2013: BMJ Case Reports
https://www.readbyqxmd.com/read/22487673/angiotensin-converting-enzyme-inhibitor-and-visceral-angio-oedema
#8
Hun Sheng Chuah, Daniel O'Donnell
Abdominal pain can be a challenging presenting complaint with a broad differential diagnosis. Medication side-effect must always be considered. Visceral angio-oedema secondary to angiotensin-converting enzyme inhibitor use can cause abdominal pain. The association of angiotensin-converting enzyme inhibitor and visceral angio-oedema is not well recognized partly because the onset of angio-oedema might be delayed for months or years after commencement of an angiotensin-converting enzyme inhibitor. The epidemiology of angio-oedema is now changing in parallel with the increasing use of angiotensin-converting enzyme inhibitors...
April 2012: Emergency Medicine Australasia: EMA
https://www.readbyqxmd.com/read/22032061/ace-inhibitor-induced-angioedema-of-the-small-intestine-a-case-report
#9
Sofie Cuypers, Stephen Van Meerbeeck, Michel De Pauw
Angiotensin-converting enzyme (ACE) inhibitors are standard medication in treating hypertension, heart failure and diabetic nephropathy. The most common side effects are cough and angioneurotic oedema of the upper airways. A less familiar side effect is the ACE inhibition-induced visceral angioedema. We report the case of a young female patient with recent diagnosis of heart failure (dilated cardiomyopathy due to viral myocarditis), who developed angioedema of the small intestine three weeks after initiating treatment with lisinopril...
October 2011: Acta Cardiologica
https://www.readbyqxmd.com/read/21852061/phenytoin-induced-drug-reaction-with-eosinophilia-and-systemic-symptoms-dress-syndrome-a-case-report-from-the-emergency-department
#10
Lindsay L Oelze, M Tyson Pillow
BACKGROUND: Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome is an uncommon but serious hypersensitivity drug reaction most frequently associated with antiepileptics. Clinical manifestations include rash, fever, and visceral organ involvement, most commonly hepatitis. The mortality rate associated with DRESS syndrome is approximately 10%, the majority due to fulminant liver failure. OBJECTIVES: We report one case of phenytoin-induced DRESS syndrome in a patient who presented to the Emergency Department (ED)...
January 2013: Journal of Emergency Medicine
https://www.readbyqxmd.com/read/21680677/hereditary-angioedema-an-unusual-cause-of-genital-swelling-presenting-to-a-genitourinary-medicine-clinic
#11
R Dhairyawan, R Harrison, M Buckland, M Hourihan
We report a case of a new diagnosis of hereditary angioedema (HAE) presenting with genital swelling to a genitourinary (GU) medicine clinic. There is often a significant delay in diagnosing HAE, but it commonly presents with genital swelling before manifesting as potentially life-threatening visceral attacks. This case highlights the fact that HAE should be considered as an important differential diagnosis of genital oedema, as early recognition may help to prevent more serious future visceral episodes.
June 2011: International Journal of STD & AIDS
https://www.readbyqxmd.com/read/21536824/visceral-angioedema-due-to-angiotensin-converting-enzyme-inhibitor-therapy
#12
REVIEW
Aleksandr Korniyenko, Carlos L Alviar, Juan P Cordova, Franz H Messerli
Visceral angioedema is an uncommon but serious complication of therapy with angiotensin-converting enzyme (ACE) inhibitors. We report a case, review the literature, and discuss the incidence, features, and clinical recognition of this condition.
May 2011: Cleveland Clinic Journal of Medicine
https://www.readbyqxmd.com/read/21427304/mdct-features-of-angiotensin-converting-enzyme-inhibitor-induced-visceral-angioedema
#13
Kalyani Vallurupalli, Kevin J Coakley
OBJECTIVE: Our objectives are to describe the CT features of angiotensin-converting enzyme (ACE) inhibitor-induced visceral angioedema and to review other conditions that may have similar findings. CONCLUSION: CT findings in a patient taking an angiotensin-converting enzyme (ACE) inhibitor help in the diagnosis and subsequent treatment of ACE inhibitor-induced visceral angioedema.
April 2011: AJR. American Journal of Roentgenology
https://www.readbyqxmd.com/read/18839624/-hereditary-angioedema-pathophysiology-genetics-symptoms
#14
REVIEW
Agnieszka Muszyńska, Ewa Janocha, Andrzej M Fal
Hereditary angioedema (HAE) is a rare but important disease because of the occurrence of life-threatening symptoms during attacks as well as due to diagnostic and therapeutic problems. Deficiency or absence of plasma protein--C1 esterase inhibitor is autosomal dominant condition and is connected with uncontrolled complement and contact systems activation which leads to the generation of vasoactive mediators, most likely bradykinin. The main syndromes are recurrent attacks of localized swelling of submucosal and subcutaneous tissue, or both...
July 2008: Polski Merkuriusz Lekarski: Organ Polskiego Towarzystwa Lekarskiego
https://www.readbyqxmd.com/read/18824924/hereditary-angioedema-in-a-family-presenting-as-transient-periarthritis
#15
Leena G Adhikesavan, Thomas P Olenginski
Hereditary angioedema (HAE) is a rare condition known to cause episodic, self-limiting, nonpruritic, nonpitting edema that involves skin and visceral organs. It may affect any external body surface including face, extremities, and genitalia. Most commonly involved viscera are gastrointestinal and respiratory systems. Patients may have severe abdominal pain because of edema of the bowel wall. This disease can cause life threatening laryngeal edema if it involves the airway.We describe a patient with HAE who was initially diagnosed with arthritis after she had recurrent edema around her peripheral joints...
October 2008: Journal of Clinical Rheumatology: Practical Reports on Rheumatic & Musculoskeletal Diseases
https://www.readbyqxmd.com/read/18325717/esophageal-foreign-body-sensation-a-rare-presentation-of-angioedema
#16
Matthew T Jordan, Darien Cohen
Angioedema remains a rare but potentially life-threatening complication of angiotensin-converting enzyme (ACE) inhibitor use. Most presentations involve edema of the tongue or oral pharynx. However, in recent years, a visceral form involving the gastrointestinal tract also has been described. We present the case of a rare presentation of esophageal and retropharyngeal edema related to ACE inhibitor use. A review of ACE inhibitor-related angioedema is also presented.
August 2010: Journal of Emergency Medicine
https://www.readbyqxmd.com/read/17018312/angiotensin-converting-enzyme-inhibitor-induced-visceral-angioedema
#17
REVIEW
H Marmery, S E Mirvis
No abstract text is available yet for this article.
November 2006: Clinical Radiology
https://www.readbyqxmd.com/read/16634360/-hereditary-angioedema-a-report-of-a-case-and-literature-review
#18
REVIEW
N Jiménez Saab, J Gómez Vera, J López Tiro, S Nieto Martínez, C Pliego Reyes
Hereditary angioedema is a congenital disorder with recurrent attacks of localized swelling of submucosal and subcutaneous tissue, or both caused by a deficiency of the plasma protein C1 inhibitor. It is caused by heterozygous defects in the C1 inhibitor gene located on chromosome 11q, and it has an autosomal dominant inheritance pattern. This disease afflicts 1 in 10,000 to 1 in 150,000 persons. Hereditary angioedema has been reported in all races, and no sex predominance has been found. Skin and visceral organs may be involved by the typically massive local edema...
January 2006: Revista Alergia Mexico: Organo Oficial de la Sociedad Mexicana de Alergia e Inmunología, A.C
https://www.readbyqxmd.com/read/16258215/drug-induced-isolated-visceral-angioneurotic-edema
#19
Masahiro Arakawa, Yaeko Murata, Yuya Rikimaru, Yasuhiko Sasaki
A 44-year-old woman on maintenance hemodialysis was admitted to our hospital because of severe abdominal pain. The patient had been medicated with lisinopril and valsartan for hypertension for one month prior to admission. An abdominal computerized scan (CT) showed a dilated and thickened loop of the small bowel with massive ascites and a small nodule in the jejunum. The patient's abdominal pain was thought to be due to isolated visceral angioneurotic edema induced by lisinopril and/or valsartan, and medication of these two drugs was therefore stopped...
September 2005: Internal Medicine
https://www.readbyqxmd.com/read/15039478/intermittent-visceral-edema-induced-by-long-term-enalapril-administration
#20
Katherine K Orr, James R Myers
OBJECTIVE: To describe a case of intermittent visceral angioedema associated with long-term enalapril use. CASE SUMMARY: A 72-year-old white woman developed severe abdominal pain as a result of visceral angioedema associated with long-term enalapril therapy. She had been taking enalapril 20 mg/day for 9 years prior to the first reported episodes of abdominal pain. DISCUSSION: Visceral angioedema associated with angiotensin-converting enzyme (ACE) inhibitors is a documented adverse effect...
May 2004: Annals of Pharmacotherapy
keyword
keyword
58748
1
2
Fetch more papers »
Fetching more papers... Fetching...
Read by QxMD. Sign in or create an account to discover new knowledge that matter to you.
Remove bar
Read by QxMD icon Read
×

Search Tips

Use Boolean operators: AND/OR

diabetic AND foot
diabetes OR diabetic

Exclude a word using the 'minus' sign

Virchow -triad

Use Parentheses

water AND (cup OR glass)

Add an asterisk (*) at end of a word to include word stems

Neuro* will search for Neurology, Neuroscientist, Neurological, and so on

Use quotes to search for an exact phrase

"primary prevention of cancer"
(heart or cardiac or cardio*) AND arrest -"American Heart Association"