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Dive into the research topics where Simon Strauss is active.

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Featured researches published by Simon Strauss.


Journal of Ultrasound in Medicine | 2004

Leydig Cell Tumors of the Testis Gray Scale and Color Doppler Sonographic Appearance

Zeev V. Maizlin; Alexander Belenky; Myriam Kunichezky; Judith Sandbank; Simon Strauss

Objective. To determine the gray scale and color Doppler sonographic features of Leydig cell tumors of the testis in a series of patients. Methods. We retrospectively analyzed the sonographic appearance of 10 proven Leydig cell tumors in 9 patients aged 26 to 47 years. Sonographic features that were reviewed included the size and echogenicity of the tumors, presence of cystic areas or calcifications, and distribution pattern of detectable blood flow on color or power Doppler imaging. Results. The tumors ranged from 0.4 to 3.0 cm in diameter, but most were less than 1.0 cm in diameter. In 1 testis, 2 discrete Leydig cell tumors were found. Nine (90%) of the 10 tumors were homogeneously hypoechoic. Only 1 tumor was isoechoic with the testis. None of the tumors contained calcifications. Of 8 tumors with color Doppler imaging, 7 (88%) showed a characteristic pattern of increased peripheral blood flow, which was either circumferential or punctate. Only 1 tumor was found with internal hypervascularity. Conclusions. Peripheral hypervascularity in a hypoechoic testicular tumor that has little or no internal color Doppler flow should suggest the possibility of a Leydig cell tumor, and consideration should be given to testicle‐sparing surgery.


Pediatric Nephrology | 2005

Symptomatic urinary tract infections following voiding cystourethrography

Marianna Rachmiel; M. Aladjem; Ruth Starinsky; Simon Strauss; Yael Villa; Michael Goldman

The objective of this study was to assess the frequency of symptomatic urinary tract infections (UTIs) following voiding cystourethrography (VCUG) while using prophylactic antibiotics. Medical records of 421 patients who underwent a VCUG during a period of 4xa0years were reviewed. Three hundred forty-nine had a VCUG following a febrile UTI, and 72 had the test for evaluation of hydronephrosis. All received prophylactic antibiotics and were evaluated within 7–10xa0days following the VCUG. One hundred seventy-two children (41%) had an abnormal VCUG. Seven of 421 children (1.7%) had symptoms suggestive of UTI. Two had culture negative pyuria; one had Escherichia Coli UTI, and four had Pseudomonas aeruginosa UTI. On multivariate logistic regression analysis, the risk factors contributing to the development of UTI following VCUG were the presence of vesicoureteral reflux (VUR) and its severity (odds ratio [OR] 2.52; 95% confidence interval [CI] 2.24, 2.83, p =0.001; and OR 2.32; 95% CI 2.05,2.62, p =0.04, respectively). The incidence of VCUG-induced UTI in children receiving prophylactic antibiotic therapy is low. There is a relatively high rate of Pseudomonas UTI, especially in children with moderate to severe reflux. We recommend that children with symptoms suggesting a UTI following a VCUG should be treated for Pseudomonas aeruginosa pending culture results.


Archives of Orthopaedic and Trauma Surgery | 1982

Ilio-psoas hematoma—its detection, and treatment with special reference to hemophilia

M. Heim; Henri Horoszowski; Uri Seligsohn; Uri Martinowitz; Simon Strauss

SummaryPain around the hip joint and femoral neuropathy in a patient with a bleeding coagulopathy should alert the physician to the possibility of an iliopsoas haematoma. Unfortunately this diagnosis is often missed. Clinically, reduced hip motion, a mass in the iliac fossa and alteration in the motor and sensory function of the femoral nerve may be noted. If the pain is on the right side, appendicitis must be excluded. Ultrasound is the diagnostic aid of choice, being more sensitive than computerized tomography or radioisotope investigations. Treatment should be gradual, gentle and protracted to avoid recurrent bleeding episodes.ZusammenfassungSchmerzen in der Hüftregion und N. femoralis Neuropathie bei einem Patienten mit Hämophilie sollten den Arzt auf ein mögliches Iliopsoas-Hämatom aufmerksam machen. Unglücklicherweise wird these Diagnose oft verfehlt.Klinisch feststellbar sind: reduzierte Beweglichkeit im Hüftgelenk, eine Masse in der Fossa iliacka und motorische und sensorische Veränderungen im Innervationsgebiet des N. femoralis. Bei rechtsseitigen Schmerzen muß eine Appendicitis ausgeschlossen werden. Ultraschall ist das diagnostische Hilfsmittel der Wahl; es ist empfindlicher als die Computer-Tomographie oder Radionukliduntersuchungen.Die Behandlung sollte stufenweise, vorsichtig und langsam verlaufen, um wiederholte Blutungen zu verhindern.


Journal of Ultrasound in Medicine | 1998

Dissecting Aneurysm of the Superior Mesenteric Artery: Flow Dynamics by Color Doppler Sonography

Tsvi Dushnitsky; Amir Peer; Ludmila Katzenelson; Simon Strauss

Spontaneous dissection of the SMA is a rare occurrence, especially when not associated with aortic dissection.1 Only sporadic case reports of the sonographic demonstration of isolated spontaneous dissection of the SMA have been published,2,3 and for the most part color Doppler imaging is not included. We report the sonographic findings in an asymptomatic patient with isolated dissection of an SMA aneurysm and discuss the unique flow dynamics seen by color Doppler sonography. CASE REPORT


Urologic Oncology-seminars and Original Investigations | 2012

Testicular sparing surgery for small masses

Yaniv Shilo; Amnon Zisman; Orit Raz; Erez Lang; Simon Strauss; Judith Sandbank; Michael Segal; Yoram I. Siegel; Dan Leibovici

OBJECTIVESnTo determine the proportion of benign testicular lesions among candidates for testicular sparing surgery (TSS) and to assess the safety and efficacy of this procedure.nnnMETHODS AND MATERIALSnSixteen patients underwent surgical exploration for testicular tumors with TSS intent in our center. Surgery was performed via an inguinal approach with temporary cord occlusion and frozen section (FS) analysis of the lesions. Benign findings allowed for TSS, whereas cancer prompted total orchiectomy.nnnRESULTSnThe lesions measured 8-25 mm in the largest diameter. Eleven of the 16 lesions were benign (69%) and TSS was accomplished in these cases. Complete concordance was observed between the results of FS and permanent sections. Of the 5 patients with cancer, 3 had pure seminoma, and embryonal carcinoma and teratoma were found in 1 patient, each. Surveillance was applied in 4 of these patients, and chemotherapy was used in the patient with embryonal carcinoma. With an average follow-up duration of 48 months, all are alive and free of disease. All 11 patients in whom TSS was accomplished had an uneventful postoperative course, and with an average follow-up duration of 28 months, 9 have normal scrotal physical examination and ultrasound, whereas 2 patients were lost to follow-up.nnnCONCLUSIONSnSixty-nine percent of testicular lesions under 25 mm are benign. TSS is safe and effective in patients with small benign lesions. Cancer is reliably detected by FS, and testicular exploration is not associated with local or distant recurrence in any of our patients.


Journal of Pediatric Surgery | 2008

Familial wandering spleen: a first instance

Anna Ben Ely; Emmanuelle Seguier; Gad Lotan; Simon Strauss; Gabriela Gayer

We report on 2 sisters presenting with acute torsion of a wandering spleen within a 3-year interval. The diagnosis was made preoperatively by computed tomography (CT) in both cases. A high index of suspicion because of our experience with the first patient, who underwent splenectomy, enabled a correct early diagnosis in the sibling. On urgent surgery, reversible ischemic changes were found, and detorsion and splenopexy resulted in preservation of the spleen.


European Journal of Radiology | 1992

Use of percutaneous nephrostomy in hydronephrosis of pregnancy

Amir Peer; Simon Strauss; Ella Witz; Hana Manor; Abraham Eidelman

Traditional methods of urinary diversion in pregnancy include retrograde passage of ureteral catheter or stents and operative nephrostomy. These techniques are, however, associated with the use of anesthesia, are technically difficult to perform, and may induce labor. We report the use of percutaneous nephrostomy in four pregnant patients, two with obstruction due to ureteral calculi and two with infected hydronephrosis. The procedure provided rapid relief from pain and pyosepsis, and allowed uneventful continuation of the pregnancy to full-term, with preservation of renal function.


Nephron | 1993

Hyperoxaluria Is Not a Cause of Nephrocalcinosis in Phosphate-Treated Patients with Hereditary Hypophosphatemic Rickets

Martin Tieder; Judith Blonder; Simon Strauss; Uri Shaked; Joseph Maor; Daniela Gabizon; Hana Manor; Ben-Ami Sela

The treatment of X-linked hypophosphatemia (XLH) consists of phosphate and vitamin D3 derivatives. Transient hypercalciuria and hypercalcemia are well-known signs of vitamin D intoxication. Despite urinary calcium excretion control, the danger of nephrocalcinosis in treated patients has been emphasized. It has recently been suggested that hyperoxaluria might be a causative factor of nephrocalcinosis other than calcium in phosphate-treated XLH patients. We measured urinary oxalate and phosphate excretion in 12 patients with the syndrome of hereditary hypophosphatemic rickets with hypercalciuria (HHRH) receiving only oral phosphates and in 5 XLH patients receiving both oral phosphates and vitamin D. No correlation was found between the dosage of phosphate supplements or urinary phosphate excretion and urinary oxalate excretion, in either group of patients. Nephrocalcinosis, presenting as hyperechogenicity of the medullary pyramids, was found in 2 of the 5 XLH patients and only in 2 HHRH patients who had been treated with excessive doses of vitamin D2 and calcium, prior to the true diagnosis being established. We conclude: (1) hyperoxaluria is not a cause of nephrocalcinosis in phosphate-treated patients with hereditary hypophosphatemic rickets; (2) prolonged phosphate treatment alone does not induce nephrocalcinosis in HHRH patients, and (3) we believe that in XLH patients, nephrocalcinosis is essentially due to vitamin D overdosage at some stage, or noncompliance in phosphate intake, leading to repeated undetected hypercalciuric periods.


Journal of Clinical Ultrasound | 2011

Sonographic features of intravascular papillary endothelial hyperplasia (Masson's tumor) in the forearm

Oleg Lysyy; Ignat Schwartz; Yehuda Kolander; Simon Strauss

Intravascular papillary endothelial hyperplasia, also known as Massons tumor, is a benign, vascular lesion in which there is papillary proliferation of endothelial cells. The lesion presents as a palpable soft‐tissue mass, often located within normal or dilated vascular spaces, and may be mistaken for a sarcomatous tumor on imaging. We present the case of an intravascular papillary endothelial hyperplasia in the forearm, with a remarkable appearance on color Doppler sonography, and suggest that this entity will be encountered more frequently by sonologists in the future.


Urologic Oncology-seminars and Original Investigations | 2012

The predominance of benign histology in small testicular masses.

Yaniv Shilo; Amnon Zisman; Arie Lindner; Orit Raz; Simon Strauss; Yoram I. Siegel; Michael Segal; Judith Sandbank; Dan Leibovici

OBJECTIVESnTo evaluate the concordance between testicular tumor size and benign histology in order to identify a cut-off size, below which the rate of benign lesions would be highest.nnnMETHODS AND MATERIALSnDuring the years 1995-2008, we performed 131 consecutive testicular operations for testicular tumors. Ten of these were testicular preserving surgery, whereas the other 121 patients had radical orchiectomy. We searched for the rate of benign lesions in the following 3 groups of tumor diameter: 10 mm or less, 11-20 mm, and greater than 20 mm. ROC analysis was used to find the optimal size cut-off below which the rate of benign lesions would be highest.nnnRESULTSnBenign lesions were found in 11 patients (8%), including epidermoid cyst (n = 4), Leydig cell tumor (n = 3), fibrosis (n = 1), adenomatoid tumor (n = 2), and 1 patient with a simple cyst. Small tumor size strongly correlated with benign histology. The mean diameter of benign vs. malignant lesions was 15 mm and 41 mm, respectively (P < 0.05). The rate of benign lesions in tumors with a diameter of 10 mm or less, 11-20 mm and greater than 20 mm was 50%, 17%, and 2%, respectively. Receiver Operating characteristic (ROC) analysis with 87% sensitivity and 83% specificity revealed a cut-off value of 18.5 mm tumor diameter below which the proportion of benign lesions was 38.5% compared with 2% above it (P < 0.05).nnnCONCLUSIONSnWhile benign lesions comprise only 8% of all testicular tumors, their proportion among small lesions is much higher. With a size cut-off of 18.5 mm, 38.5% of smaller lesions are benign. These findings support consideration of testicular exploration for small testicular lesions aiming at preservation rather than predetermined radical orchiectomy.

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Dan Leibovici

University of Texas MD Anderson Cancer Center

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