scholarly journals Hinman syndrome

2020 ◽  
Author(s):  
Keyword(s):  
Hinman Syndrome

Summary of the Annual Meeting Section on Urology, American Academy of Pediatrics

PEDIATRICS ◽  
1991 ◽  
Vol 88 (2) ◽  
pp. 406-411
Author(s):  
Barry A. Kogan
Keyword(s):  
New York ◽  
American Academy ◽  
Annual Meeting ◽  
San Francisco ◽  
Wilms Tumor ◽  
Disease Free Survival ◽  
Pediatric Urology ◽  
American Academy Of Pediatrics ◽  
Hinman Syndrome ◽  
Tract Infections

Members of the Section on Urology of the American Academy of Pediatrics met for 2½ days in conjunction with the 59th Annual Meeting of the American Academy of Pediatrics in Boston, Massachusetts, October 6 to October 8, 1990. The meeting was presided over by Chairperson David T. Mininberg of Cornell University, New York. The papers presented at this meeting that are of interest to the practicing pediatrician are summarized here according to topic. The Pediatric Urology Medal, awarded to an individual who has made outstanding contributions to the field of pediatric urology, was presented to Dr Frank Hinman, Jr. of the University of California. San Francisco. Dr Hinman was recognized for his many years of work dedicated to improving the urologic care of children. A foremost clinician, teacher, and researcher, he has contributed particularly to the understanding of urinary tract infections and bladder dysfunction in children, particularly those children who have "Hinman Syndrome," the non-neurogenic neurogenic bladder. Dr Hinman has been a strong advocate for the specialized urologic care of children for many years. GENITOURINARY NEOPLASMS Wilms' tumor is one disease in which there has been impressive progress in recent years, particularly with the advent of effective chemotherapy that has enabled these children to have increased disease-free survival. Montgomery and co-workers from the Mayo Clinic reviewed the experience of patients with bilateral Wilms' tumor during the past 16 years. Ten-year survival was 69%. Seventy-five percent of the failures resulted from recurrent disease (which generally occurred early), and 25% resultes from treatment complications.

scholarly journals De Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantation

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
Arnaud Devresse ◽  
Martine de Meyer ◽  
Selda Aydin ◽  
Karin Dahan ◽  
Nada Kanaan
Keyword(s):  
Kidney Transplantation ◽  
De Novo ◽  
Alternative Pathway ◽  
Factor H ◽  
Complement Factor ◽  
Haemolytic Uremic Syndrome ◽  
Hinman Syndrome ◽  
Uremic Syndrome ◽  
Stage Renal Disease ◽  
End Stage

De novo thrombotic microangiopathy (TMA) can occur after kidney transplantation. An abnormality of the alternative pathway of complement must be suspected and searched for, even in presence of a secondary cause. We report the case of a 23-year-old female patient who was transplanted with a kidney from her mother for end-stage renal disease secondary to Hinman syndrome. Early after transplantation, she presented with 2 episodes of severe pyelonephritis, associated with acute kidney dysfunction and biological and histological features of TMA. Investigations of the alternative pathway of the complement system revealed atypical haemolytic uremic syndrome secondary to complement factor I mutation, associated with mutations in CD46 and complement factor H related protein genes. Plasma exchanges followed by eculizumab injections allowed improvement of kidney function without, however, normalization of creatinine.

Hinman Syndrome: Long Term Follow up of 14 Cases

2007 ◽  
Vol 48 (10) ◽  
pp. 1058
Author(s):  
Dong Hoon Lee ◽  
Yong Soo Kim ◽  
Hye Young Lee ◽  
Sang Won Han
Keyword(s):  
Hinman Syndrome ◽  
Long Term Follow Up

Advanced Transitional Cell Carcinoma of the Bladder in a 16-Year-Old Girl With Hinman Syndrome

Urology ◽  
2012 ◽  
Vol 80 (5) ◽  
pp. 1141-1143 ◽  
Author(s):  
Anas I. Ghousheh ◽  
Charles T. Durkee ◽  
Travis W. Groth
Keyword(s):  
Transitional Cell Carcinoma ◽  
Cell Carcinoma ◽  
Transitional Cell ◽  
Hinman Syndrome ◽  
Carcinoma Of The Bladder

scholarly journals Hinman syndrome in 7-year-old child: a clinical case

2018 ◽  
pp. 110-112
Author(s):  
V.D. Malischuk ◽  
◽  
T.P. Ovsiychuk ◽  
S.V. Komarovskiy ◽  
F.O. Gavrilyuk ◽  
...  
Keyword(s):  
Clinical Case ◽  
Hinman Syndrome

scholarly journals An Unusual Case of Syringohydromyelia Presenting with Neurogenic Bladder

2019 ◽  
Vol 07 (01) ◽  
pp. e79-e82
Author(s):  
Antonella Geljic ◽  
Slaven Abdovic ◽  
Fran Stampalija ◽  
Lana Loncar ◽  
Batos A. Tripalo ◽  
...  
Keyword(s):  
Urinary Retention ◽  
Urinary Catheter ◽  
Outlet Obstruction ◽  
Conus Medullaris ◽  
Sensory Loss ◽  
Clean Intermittent Catheterization ◽  
Neurological Sequelae ◽  
Hinman Syndrome ◽  
Tract Infections

AbstractWe report the case of a 4-year-old boy who first presented with acute pyelonephritis at the age of 6 months. Diagnostic workup revealed high-grade bilateral vesicourethral reflux (VUR). At the age of 18 months, a bulking agent was used to treat bilateral VUR. Since the VUR persisted, an open bilateral Lich-Gregoir procedure was done at the age of 3 years. Immediately after surgery, he developed acute urinary retention with hydronephrosis that resolved with the placement of dwelling urinary catheter. After removal of the catheter urinary retention relapsed so placement of suprapubic urinary catheter was indicated since he did not have sensory loss. He was started with tamsulosin (α − 1-blocker) and prophylactic antibiotics. Urodynamics were performed and suggested bladder outlet obstruction. On the basis of previous urethroscopy and the absence of neurological sequelae, the differential diagnosis of Hinman syndrome was made. After removal of the suprapubic catheter, clean intermittent catheterization was started and α-blocker continued. However, magnetic resonance imaging of the brain and the spinal cord revealed syringohydromyelia extending from thoracic spine (Th5) to conus medullaris with 6 to 7 mm in diameter. Electromyoneurogram was normal. After a follow-up of 3 years, the hydronephrosis has resolved. The patient is on clean intermittent catherization and has no urinary tract infections.

scholarly journals Hypertensive urgency in nephrogenic diabetes insipidus with concomitant Hinman syndrome

2019 ◽  
Vol 12 (7) ◽  
pp. e229095
Author(s):  
Yu Guang Tan ◽  
Daniel Wei Keong Chan ◽  
Fabian Kok Peng Yap ◽  
Te-Lu Yap
Keyword(s):  
Renal Impairment ◽  
Diabetes Insipidus ◽  
Nephrogenic Diabetes Insipidus ◽  
Failure To Thrive ◽  
Age Group ◽  
Urinary System ◽  
Hypertensive Urgency ◽  
Anatomical Changes ◽  
Hinman Syndrome ◽  
Concentrate Urine

Diabetes insipidus is a syndrome characterised by the inability to conserve water or concentrate urine, leading to excessive excretion of urine. In congenital nephrogenic diabetes insipidus (CNDI), common presentations include failure to thrive, polydipsia, polyuria and dehydration. The long trajectory of the disease, coupled with psycho-behavioural changes as a child grows, can precipitate a period of non-adherence despite initial optimal control, especially in the adolescent age group. Social inconvenience of repeated voiding and nocturnal disturbances can lead to adapted urine holding behaviour, also known as non-neurogenic neurogenic bladder (Hinman syndrome). Anatomical changes in the urinary system, such as bladder trabeculation and hydroureteronephrosis, can subsequently give rise to functional renal impairment. We present a case of CNDI with concomitant Hinman syndrome, resulting in acute renal impairment and hypertensive emergency. We aim to raise awareness of the association between these two entities.

Hinman Syndrome

1994 ◽  
Vol 19 (8) ◽  
pp. 747-748 ◽  
Author(s):  
ALAN E. HARRIS ◽  
MORAKINYO A. O. TONEY
Keyword(s):  
Hinman Syndrome

Hinman syndrome: A vicious cycle

Urology ◽  
1993 ◽  
Vol 42 (3) ◽  
pp. 317-319 ◽  
Author(s):  
Emilia Phillips ◽  
David T. Uehling
Keyword(s):  
Vicious Cycle ◽  
Hinman Syndrome

Distention of the posterior urethra: association with nonneurogenic neurogenic bladder (Hinman syndrome).

Radiology ◽  
1992 ◽  
Vol 185 (1) ◽  
pp. 113-117 ◽  
Author(s):  
J F Johnson ◽  
R J Hedden ◽  
M L Piccolello ◽  
J Wacksman
Keyword(s):  
Neurogenic Bladder ◽  
Hinman Syndrome ◽  
Posterior Urethra
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