scholarly journals Endoscopic Findings in Loin Pain Hematuria Syndrome: Concentric Clot in Calyceal Fornices

2008 ◽  
Vol 2008 ◽  
pp. 1-3 ◽  
Author(s):  
Benjamin K. Canales ◽  
Andrew Windsperger ◽  
Stephen Lukasewycz ◽  
Manoj Monga

The loin pain hematuria syndrome (LPHS) creates a considerable burden, both for patients afflicted with the disease and for those involved in medical management and diagnosis. To date, the diagnosis of LPHS remains one of exclusion, with some speculation regarding the extent of actual pathology. We report ureteroscopic findings in 2 cases of LPHS. These findings provide objective confirmation of underlying pathology in a difficult-to-manage disease process.

2020 ◽  
pp. 141-144
Author(s):  
Sarang Koushik

Background: Loin pain hematuria syndrome (LPHS) is a rare syndrome presenting with chronic unilateral or bilateral flank pain and gross or microscopic hematuria. Case Report: We present a case of LPHS in a male with past medical history of atrial fibrillation, Barrett’s esophagus, and loin pain hematuria syndrome who initially presented to our medical facility with gross hematuria, intractable left flank pain, and non-bloody emesis. Our case exemplifies the challenge in managing patients with LPHS. Conclusion: Without a definitive mechanism for LPHS, current treatment focuses on symptom management. Analgesics (non-opioid and opioid) may be used orally or intravenous depending on the presence of concomitant nausea and vomiting. For patients at risk of opioid dependence, targeting afferent pain fibers originating from the kidneys and ureters has proven a successful analgesic strategy. Surgical options for renal denervation include: endovascular radiofrequency ablation, laparoscopic renal denervation, and renal auto transplant. Treatment options for this disease process include intra-ureteric bupivacaine, renal denervation, and possible spinal cord stimulation. Key words: Flank pain, loin pain hematuria syndrome, renal denervation, spinal cord stimulation


Author(s):  
Amy Lustig ◽  
Cesar Ruiz

The purpose of this article is to present a general overview of the features of drug-induced movement disorders (DIMDs) comprised by Parkinsonism and extrapyramidal symptoms. Speech-language pathologists (SLPs) who work with patients presenting with these issues must have a broad understanding of the underlying disease process. This article will provide a brief introduction to the neuropathophysiology of DIMDs, a discussion of the associated symptomatology, the pharmacology implicated in causing DIMDs, and the medical management approaches currently in use.


2021 ◽  
Vol 25 (1) ◽  
Author(s):  
Ivan Urits ◽  
Nathan Li ◽  
Amnon A. Berger ◽  
Paul Walker ◽  
Brendan Wesp ◽  
...  

ESC CardioMed ◽  
2018 ◽  
pp. 1728-1729
Author(s):  
Patrizio Lancellotti ◽  
Stella Marchetta

Non-bacterial thrombotic endocarditis (NBTE) is characterized by the presence of sterile vegetations on cardiac valves that consist of fibrin and platelet aggregates. These vegetations are neither associated with bacteraemia nor with destructive changes of the underlying valve. The diagnosis of NBTE relies on strong clinical suspicion in the context of (a) a disease process known to be associated with NBTE, (b) the presence of a heart murmur, (c) a negative blood culture, (d) the presence of vegetations not responding to antibiotic treatment, and (e) evidence of multiple systemic emboli. The same initial diagnostic work-up as for infective endocarditis is recommended. Serial blood cultures, exhaustive haematological and coagulation studies, and a comprehensive echocardiography should be performed. The management of NBTE is challenging and a tailored approach should be advocated. It should first focus on the underlying pathology. In the absence of contraindications, an anticoagulation treatment should be given. Surgical intervention is not recommended unless the patient has clear indications (i.e. heart failure due to valve dysfunction).


2019 ◽  
Vol 51 (6) ◽  
pp. 927-930
Author(s):  
Jeffrey Campsen ◽  
Mitchell R. Bassett ◽  
Ryan O’Hara ◽  
Robin D. Kim ◽  
Eryberto Martinez ◽  
...  

2002 ◽  
Vol 81 (11) ◽  
pp. 785-789 ◽  
Author(s):  
Robert F. Spencer ◽  
Aristides Sismanis ◽  
Jefferson K. Kilpatrick ◽  
Wayne T. Shaia

We conducted a study to determine whether vestibular nerves inpatients with unilateral Ménière's disease whose symptoms are refractory to medical management exhibit neuropathologic changes. We also endeavored to determine whether retrocochlear abnormalities are primary or secondary factors in the disease process. To these ends, we obtained vestibular nerve segments from five patients during retrosigmoid (posteriorfossa) neurectomy, immediately fixed them, and processed them for light and electron microscopy. We found that all five segments exhibited moderate to severe demyelination with axonal sparing. Moreover, we noted that reactive astrocytes produced an extensive proliferation of fibrous processes and that the microglia assumed a phagocytic role. We conclude that the possible etiologies of demyelination include viral and/or immune-mediated factors similar to those seen in other demyelinating diseases, such as multiple sclerosis and Guillain-Barré syndrome. Our findings suggest that some forms of Ménière's disease that are refractory to traditional medical management might be the result of retrocochlear pathology that affects the neuroglial portion of the vestibular nerve.


1998 ◽  
Vol 160 (4) ◽  
pp. 1232-1236 ◽  
Author(s):  
JOSEPH L. CHIN ◽  
DEBRA KLOTH ◽  
STEPHEN E. PAUTLER ◽  
MICHAEL MULLIGAN

1998 ◽  
pp. 1232-1235 ◽  
Author(s):  
JOSEPH L. CHIN ◽  
DEBRA KLOTH ◽  
STEPHEN E. PAUTLER ◽  
MICHAEL MULLIGAN

1988 ◽  
Vol 9 (1) ◽  
pp. 155-157 ◽  
Author(s):  
John E. Reifsteck ◽  
John C. Holder ◽  
Gin Chung Liu ◽  
Ernest J. Ferris ◽  
Alex E. Finkbeiner

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