Median nerve neuropraxia by a large false brachial artery aneurysm

Vascular ◽  
2013 ◽  
Vol 22 (5) ◽  
pp. 378-380 ◽  
Author(s):  
Niki Lijftogt ◽  
Ernst Cancrinus ◽  
Erwin LJ Hoogervorst ◽  
Rob HW van de Mortel ◽  
Jean-Paul PM de Vries

Peripheral nerve compression is a rare complication of an iatrogenic false brachial artery aneurysm. We present a 72-year-old patient with median nerve compression due to a false brachial artery aneurysm after removal of an arterial catheter. Surgical exclusion of the false aneurysm was performed in order to release traction of the median nerve. At 3-month assessment, moderate hand recovery in function and sensibility was noted. In the case of neuropraxia of the upper extremity, following a history of hospital stay and arterial lining or catheterization, compression due to pseudoaneurysm should be considered a probable cause directly at presentation. Early recognition and treatment is essential to avoid permanent neurological deficit.

2019 ◽  
Vol 21 (5) ◽  
pp. 799-802 ◽  
Author(s):  
Elisa Maria Schilling ◽  
Malte Weinrich ◽  
Thomas Heller ◽  
Sebastian Koball ◽  
Andreas Neumann

Our patient exhibited a large tumor on his right upper arm where his former dialysis access site had been. X-ray, Doppler ultrasound, and magnetic resonance imaging scan could not fully reveal the nature of that tumor. Eventually, a surgical approach showed a giant aneurysm of the inflowing brachial artery to a partially obliterated arteriovenous fistula. This case highlights the importance of ongoing care for patients with arteriovenous shunts. Even arteriovenous fistulas, that are obliterated or no longer in use, can, especially when immunosuppressant therapy and other vascular risk factors are added to the overall cardiovascular risk, transform and endanger the health of our patients.


1994 ◽  
Vol 19 (3) ◽  
pp. 289-291 ◽  
Author(s):  
K. DESTA ◽  
M. O’SHAUGHNESSY ◽  
M. A. P. MILLING

A 70-year-old woman presented with median nerve compression secondary to enlarged supratrochlear lymph nodes infiltrated with malignant non-Hodgkin’s lymphoma. Peripheral nerve compression is rarely seen in this condition. The management and prognosis are discussed.


2004 ◽  
Vol 50 (3) ◽  
pp. 75-76
Author(s):  
Fernando Ruiz Santiago ◽  
Pilar Jiménez Villares ◽  
Juan Miguel Tristán Fernández ◽  
Fabiola Muñoz Parra

HAND ◽  
1978 ◽  
Vol os-10 (2) ◽  
pp. 167-175 ◽  
Author(s):  
John Chalmers

summary This paper presents two anatomical variants as possible causes of peripheral nerve compression — the median nerve by a persisting median artery and the ulnar nerve by the muscle anconeous epitrochlearis.


2010 ◽  
Vol 44 (8) ◽  
pp. 691-692 ◽  
Author(s):  
Stephen O'Neill ◽  
Mark E. O'Donnell ◽  
Anton Collins ◽  
Denis W. Harkin

2020 ◽  
Vol 4 (Supplement_1) ◽  
Author(s):  
Priyanka Majety ◽  
Richard D Siegel

Abstract Background: Hypertriglyceridemia (HTG) is a well-established cause of acute pancreatitis (AP) in up to 14% of all cases & up to 56% cases during pregnancy. The triad of HTG, Diabetic ketoacidosis (DKA) and AP is rarely seen posing diagnostic challenges. Early recognition of HTG-induced pancreatitis (HTGP) is important to provide appropriate therapy & prevent recurrence. In this case series, we discuss the diagnostic challenges and clinical features of HTGP. Clinical cases: Our first patient was a 65-year-old male with a history of hypertension who presented to the ER with abdominal pain and new-onset pruritic skin rash after a heavy meal. His exam and labs were notable for a diffuse papular rash on his back, triglycerides (TG) of 7073mg/dL (normal: <150mg/dL). The rash improved with the resolution of HTG. Our second patient was a 29-year-old male with a history of alcohol dependence who was found to have AP complicated by ARDS requiring intubation. Further testing revealed that his TG was 12,862mg/dL & his sodium (Na) was 102mEq/L. Although HTG was known to cause pseudohyponatremia, it was a diagnostic challenge to estimate the true Na level. In a third scenario, a 28-year-old female with a history of T2DM on Insulin presented with nausea & abdominal pain. Labs were suggestive of DKA and lipase was normal. CT abdomen showed changes consistent with AP. The TG level that was later added on was elevated to 4413mg/dL. She was treated with insulin that improved her TG level. Discussion: We present three cases of hypertriglyceridemic pancreatitis. While the presentation can be similar to other causes of acute pancreatitis (AP), there are factors in the diagnosis and management of HTGP that are important to understand. Occasionally, physical exam findings can be suggestive of underlying HTG. In the first scenario, our patient presented with eruptive xanthomas - a sudden eruption of crops of papules that can be pruritic. They are highly suggestive of HTG, often associated with serum TG levels > 1500mg/dL. Our second patient presented with pseudohyponatremia. HTG falsely lowers Na level, by affecting the percentage of water in plasma. Identifying this condition is important to prevent possible complications from aggressive treatment. This can be corrected either by using direct ion-specific electrodes or with the formula: Na change = TG * 0.002. DKA is associated with mild-moderate HTG in 30–50% cases. This is due to insulin deficiency causing activation of lipolysis in adipocytes & decreased activity of lipoprotein lipase (LPL). However, severe HTG is a rare complication of DKA, increasing the risk of AP. Diagnosis of AP in DKA poses many challenges: the common presenting complaint of abdominal pain, non-specific hyperlipasemia in DKA. AP with DKA has also been associated with normal lipase levels. A high clinical index of suspicion is required to diagnose HTGP in patients with DKA.


2014 ◽  
Vol 28 (1) ◽  
pp. 122.e1-122.e3 ◽  
Author(s):  
Yan Ortiz-Pomales ◽  
Jennifer Smith ◽  
Jeffrey Weiss ◽  
Kevin Casey

EJVES Extra ◽  
2007 ◽  
Vol 13 (3) ◽  
pp. 44-46
Author(s):  
K. Bhatti ◽  
S. Ali ◽  
S.K. Shamugan ◽  
A.S. Ward

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