Neurogenes pulmonales Ödem (NPE) bei einem 13-jährigen Mädchen mit AV-Malformation der hinteren Schädelgrube

2007 ◽  
Vol 211 (S 1) ◽  
Author(s):  
D Wurm ◽  
W Reith ◽  
A Lindinger ◽  
S Meyer ◽  
L Gortner
Keyword(s):  
2004 ◽  
Vol 208 (S 1) ◽  
Author(s):  
C Weisser ◽  
J Micallef ◽  
R Ghisla ◽  
P Waibel
Keyword(s):  

2021 ◽  
pp. 112067212199663
Author(s):  
Marilyn A Márquez ◽  
Claudio P Juárez ◽  
Maria C Sánchez ◽  
Jose D Luna

Purpose: To report a case of a patient with NF1 presenting with ocular findings of AV malformation, multiple retinal hemorrhages, and neovascular glaucoma in the absence of retinal ischemia. Methods: Review of the medical record was conducted in accordance with the local IRBt. Results: A 60-year-old female patient with diagnosis of Neurofibromatosis type1 (NF1) and sudden decrease of vision in her left eye was found to have rubeosis iridis and high intraocular pressure (IOP). On fundus exam multiple corkscrew retinal vessels and retinal hemorrhages were present in her left eye. On Optical Coherence Tomography (OCT) the foveal hemorrhages appeared as outer layer hyperreflective retinal infiltrates whereas in the parafoveal area the hyperreflectivity was present between the RPE and neurosensory retina. Fluorescein Angiogram (FA) showed normal perfusion and no areas of leakage or ischemia. Treatment with anti-angiogenics in a timely manner correlated with a good visual outcome. Conclusions: We present a unique patient with NF1, rubeosis iridis, high IOP, and macular hemorrhages from multiple corkscrew retinal vessels in a well perfused retina, who underwent treatment with a single dose of intravitreal Bevacizumab and had an excellent response


2000 ◽  
Vol 15 (2) ◽  
pp. 84-86
Author(s):  
E. Erel ◽  
L. D. Wijesinghe ◽  
P. T. McCollum

Design: Case report. Setting: Vascular Surgery Department, Hull Royal Infirmary, UK. Patients: A 79-year-old man with a history of right leg ulcer and pulsatile veins. Investigations and interventions: Clinical examination revealed findings of tricuspid regurgitation. Investigations included duplex scans, CT scan, arteriography and both trans-thoracic and trans-oesophageal echocardio-graphy. These all proved inconclusive. High sapheno-femoral ligation and stripping of long saphenous vein ligation procedure resulted in healing of his ulcers within six months Conclusion: Pulsatile veins in the leg may be due to tricuspid regurgitation or AV malformation. Echocardiogram, duplex scan and angiograms can help to differentiate between the two diagnoses. In this case, the above investigations were misleading and clinical examination here played the key role.


Pneumologie ◽  
2019 ◽  
Author(s):  
F. Forster ◽  
W. Schulte

ZusammenfassungWir stellen hier eine sehr seltene, aber wichtig zu bedenkende Ursache einer pulmonalen Hämorrhagie in der Schwangerschaft vor. Eine 41-jährige Patientin stellt sich mit Hämoptysen in der 29. Schwangerschaftswoche vor, die bei Oligosymptomatik und spontanem Sistieren als unspezifisch entzündlich gedeutet werden. Bei Wiedervorstellung in der 34. Schwangerschaftswoche mit progredienter Hämoptoe sowie Schwindel erfolgt der Nachweis einer bis dahin nicht bekannten idiopathischen pulmonalen AV-Malformation, die eng interdisziplinär abgestimmt mit Bronchoskopie, Sectio caesarea, CT-Thorax und VATS/Minithorakotomie mit Segmentresektion notfallmäßig erfolgreich behandelt wird.


1977 ◽  
Vol 11 (4) ◽  
pp. 551-551 ◽  
Author(s):  
Bernard G Gauthier ◽  
Edward S Wind ◽  
Ashok C Shende ◽  
Philip Lanzkowsky ◽  
George P Pillari
Keyword(s):  

2020 ◽  
Vol 11 (4) ◽  
pp. 7432-7435
Author(s):  
Athulya Subhash ◽  
Anukrishna V P ◽  
Velayudhan K K ◽  
Sayyid Moidu Mon C ◽  
Remya Reghu

Rheumatic heart disease(RHD) is an inflammatory disease that mostly occurs in children of 5-15 years old. The major complications of RHD include arrhythmias, especially atrial fibrillation, stroke, infective endocarditis, cardiac failure, and also noted that problems increased in pregnancy. This is a rare case of RHD and urosepsis in a 67- year- old patient with a known history of cerebrovascular accident, pulmonary Arteriovenous(AV) malformation, acute renal failure, and hyponatremia presented to the emergency department with complaints of fever, severe breathlessness, and cough. The patient initially showed clinical manifestations of elevated inflammatory markers, neutrophilic leucocytosis, and hyponatremia, indicating septic shock. Our patient had been empirically treated with Piperacillin-Tazobactam because of the clinical features of urosepsis with septic shock. Based on Bronchoalveolar lavage(BAL) culture with non-fermenter Presumptive Acinetobacter and Klebsiella species and culture sensitivity report antibiotics were changed to Colistin and meropenem. The presence of carbapenem-resistant Klebsiella pneumoniae (CR Kp) entails stopping meropenem and adding tigecycline. Further creatinine clearance declined, and the drug Colistin was changed to Polymixin B. Meropenem was readministered based on the culture reports with scanty growth of multidrug-resistant Proteus mirabilis. Rational use of antibiotics along with the appropriate supportive measures is a meaningful measure in treating a rare and complicated condition of RHD with urosepsis.


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