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  1. Article: Unilateral multicystic renal dysplasia: Prenatal diagnosis on ultrasound.

    Pandya, Vaidehi K / Sutariya, Harsh C

    Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia

    2017  Volume 28, Issue 4, Page(s) 916–920

    Abstract: Multicystic renal dysplasia (MCRD) is the most common cause of abnormally enlarged kidney, diagnosed on antenatal ultrasound examination. It is an abnormality of the embryonic development in which the renal parenchyma is substituted by nonfunctioning ... ...

    Abstract Multicystic renal dysplasia (MCRD) is the most common cause of abnormally enlarged kidney, diagnosed on antenatal ultrasound examination. It is an abnormality of the embryonic development in which the renal parenchyma is substituted by nonfunctioning renal tissue made up of cysts which do not communicate with each other. Vesicoureteric reflux (VUR), pelviureteric junction obstruction, vesicoureteric junction obstruction, and ureterocele are the most commonly seen abnormalities in contralateral kidney. Here, we report a case of prenatal diagnosis of unilateral MCRD with VUR in contralateral kidney. In conclusion, we want to emphasize optimal use of ultrasound imaging to detect such abnormalities as early as possible to guide the proper management.
    MeSH term(s) Cystography ; Female ; Humans ; Hydronephrosis/diagnostic imaging ; Infant, Newborn ; Kidney/abnormalities ; Kidney/diagnostic imaging ; Kidney/physiopathology ; Male ; Multicystic Dysplastic Kidney/diagnostic imaging ; Multicystic Dysplastic Kidney/physiopathology ; Multicystic Dysplastic Kidney/therapy ; Predictive Value of Tests ; Pregnancy ; Prognosis ; Radionuclide Imaging ; Ultrasonography, Prenatal ; Urination ; Vesico-Ureteral Reflux/diagnostic imaging ; Vesico-Ureteral Reflux/physiopathology ; Vesico-Ureteral Reflux/therapy
    Language English
    Publishing date 2017-07-26
    Publishing country Saudi Arabia
    Document type Case Reports
    ZDB-ID 1379955-1
    ISSN 1319-2442
    ISSN 1319-2442
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 4735: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  2. Article: Renal Papillary Necrosis: Role of Radiology.

    Sutariya, Harsh C / Pandya, Vaidehi K

    Journal of clinical and diagnostic research : JCDR

    2016  Volume 10, Issue 1, Page(s) TD10–2

    Abstract: Renal Papillary Necrosis (RPN) is idefined as Ischemic necrobiosis of the papilla in the medulla of the kidneys. Variety of etiological factors are recognized which cause papillary necrosis, such as analgesic nephropathy, diabetes mellitus, urinary ... ...

    Abstract Renal Papillary Necrosis (RPN) is idefined as Ischemic necrobiosis of the papilla in the medulla of the kidneys. Variety of etiological factors are recognized which cause papillary necrosis, such as analgesic nephropathy, diabetes mellitus, urinary obstruction and sickle cell haemoglobinopathy. The early diagnosis of RPN is important to improve prognosis and reduce morbidity. Radiological Imaging offers early diagnosis and can guide prompt treatment of papillary necrosis and can minimize a decline in renal function. Here we report three cases of RPN with typical imaging findings. One of them was diabetic and hypertensive female with recurrent Urinary tract Infections and other was a male with no known co-morbidity. Both of them were diagnosed to have renal papillary necrosis on CT scan and were managed operatively and conservatively, respectively. Third case was a healthy female being investigated to be renal donor for her son. Here RPN was an incidental finding and was treated conservatively. Thus CT scan could detect it pre-operatively and complications due to transplantation of a kidney with papillary necrosis were avoided. So, we want to emphasize the importance of Radiology, particularly CT scanning in detection of RPN and to guide early and prompt treatment.
    Language English
    Publishing date 2016-01-01
    Publishing country India
    Document type Case Reports
    ZDB-ID 2775283-5
    ISSN 0973-709X ; 2249-782X
    ISSN (online) 0973-709X
    ISSN 2249-782X
    DOI 10.7860/JCDR/2016/15092.7091
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Disseminated Tuberculosis Involving Allograft in a Renal Transplant Recipient.

    Sutariya, Harsh C / Panchal, Tejal N / Pandya, Vaidehi K / Patel, Kajal N

    Journal of global infectious diseases

    2016  Volume 8, Issue 1, Page(s) 55–56

    Language English
    Publishing date 2016-02-17
    Publishing country India
    Document type Journal Article
    ZDB-ID 2545454-7
    ISSN 0974-8245 ; 0974-777X
    ISSN (online) 0974-8245
    ISSN 0974-777X
    DOI 10.4103/0974-777X.176151
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Unilateral multicystic renal dysplasia

    Vaidehi K Pandya / Harsh C Sutariya

    Saudi Journal of Kidney Diseases and Transplantation, Vol 28, Iss 4, Pp 916-

    Prenatal diagnosis on ultrasound

    2017  Volume 920

    Abstract: Multicystic renal dysplasia (MCRD) is the most common cause of abnormally enlarged kidney, diagnosed on antenatal ultrasound examination. It is an abnormality of the embryonic development in which the renal parenchyma is substituted by nonfunctioning ... ...

    Abstract Multicystic renal dysplasia (MCRD) is the most common cause of abnormally enlarged kidney, diagnosed on antenatal ultrasound examination. It is an abnormality of the embryonic development in which the renal parenchyma is substituted by nonfunctioning renal tissue made up of cysts which do not communicate with each other. Vesicoureteric reflux (VUR), pelviureteric junction obstruction, vesicoureteric junction obstruction, and ureterocele are the most commonly seen abnormalities in contralateral kidney. Here, we report a case of prenatal diagnosis of unilateral MCRD with VUR in contralateral kidney. In conclusion, we want to emphasize optimal use of ultrasound imaging to detect such abnormalities as early as possible to guide the proper management.
    Keywords Medicine ; R
    Language English
    Publishing date 2017-01-01T00:00:00Z
    Publisher Wolters Kluwer Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article: Bilateral Renal Lymphangiectasia.

    Pandya, Vaidehi K / Shah, Maulin K / Gandhi, Shruti P / Patel, Himanshu V

    Journal of clinical and diagnostic research : JCDR

    2016  Volume 10, Issue 9, Page(s) TD01–TD02

    Abstract: Renal Lymphangiectasia (RLM) is very rare benign lymphatic malformation. It can be misdiagnosed for other cystic renal masses, most commonly polycystic kidneys. Though incidentally found in most cases, it may be the cause for hypertension and renal ... ...

    Abstract Renal Lymphangiectasia (RLM) is very rare benign lymphatic malformation. It can be misdiagnosed for other cystic renal masses, most commonly polycystic kidneys. Though incidentally found in most cases, it may be the cause for hypertension and renal failure in undiagnosed patients. Here, we report a case of an adult asymptomatic male with bilateral RLM which was detected as an incidental finding on ultrasound. Confirmation by CT-scan and laboratory diagnosis of aspirated fluid was done, and patient was managed conservatively.
    Language English
    Publishing date 2016-09-01
    Publishing country India
    Document type Case Reports
    ZDB-ID 2775283-5
    ISSN 0973-709X ; 2249-782X
    ISSN (online) 0973-709X
    ISSN 2249-782X
    DOI 10.7860/JCDR/2016/19475.8409
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Disseminated tuberculosis involving allograft in a renal transplant recipient

    Harsh C Sutariya / Tejal N Panchal / Vaidehi K Pandya / Kajal N Patel

    Journal of Global Infectious Diseases, Vol 8, Iss 1, Pp 55-

    2016  Volume 56

    Keywords Infectious and parasitic diseases ; RC109-216 ; Internal medicine ; RC31-1245 ; Medicine ; R
    Language English
    Publishing date 2016-01-01T00:00:00Z
    Publisher Wolters Kluwer Medknow Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    Full text online

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  7. Article ; Online: Bilateral Renal Lymphangiectasia

    Vaidehi K Pandya / Maulin K Shah / Shruti P Gandhi / Himanshu V Patel

    Journal of Clinical and Diagnostic Research, Vol 10, Iss 9, Pp TD01-TD

    2016  Volume 02

    Abstract: Renal Lymphangiectasia (RLM) is very rare benign lymphatic malformation. It can be misdiagnosed for other cystic renal masses, most commonly polycystic kidneys. Though incidentally found in most cases, it may be the cause for hypertension and renal ... ...

    Abstract Renal Lymphangiectasia (RLM) is very rare benign lymphatic malformation. It can be misdiagnosed for other cystic renal masses, most commonly polycystic kidneys. Though incidentally found in most cases, it may be the cause for hypertension and renal failure in undiagnosed patients. Here, we report a case of an adult asymptomatic male with bilateral RLM which was detected as an incidental finding on ultrasound. Confirmation by CT-scan and laboratory diagnosis of aspirated fluid was done, and patient was managed conservatively.
    Keywords ct scan ; polycystic kidneys ; ultrasound ; Medicine ; R
    Language English
    Publishing date 2016-09-01T00:00:00Z
    Publisher JCDR Research and Publications Private Limited
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    Full text online

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  8. Article ; Online: Role of CT scan in diagnosis of renal lymphangiectasia: our single-center experience.

    Pandya, Vaidehi K / Sutariya, Harsh C / Gandhi, Shruti P / Khemchandani, Sajni I / Patel, Himanshu V / Shah, Maulin K

    Renal failure

    2017  Volume 39, Issue 1, Page(s) 533–539

    Abstract: Background: Renal lymphangiectasia is rarely reported benign renal disorder of lymphatic malformation. Though found incidentally; it presents with nonspecific symptoms and shows characteristic findings in radiological imaging studies.: Aim: Here, we ... ...

    Abstract Background: Renal lymphangiectasia is rarely reported benign renal disorder of lymphatic malformation. Though found incidentally; it presents with nonspecific symptoms and shows characteristic findings in radiological imaging studies.
    Aim: Here, we report eight patients with symptoms, laboratory and imaging findings compatible with renal lymphangiectasia. This report describes clinical and laboratory characteristics, treatment, Imaging findings and outcome of a series of patients with renal lymphangiectasia and reviews the literature.
    Methods and material: Eight patients (mean age 45 years, male:female ratio 3:1) from 1st January 2011 to 30th June 2016; showing renal lymphangiectasia as incidental finding on CT IVP were included in the series. Imaging and laboratory findings were reviewed. Two out of eight patients (25%) underwent aspiration of collection and laboratory findings confirmed the diagnosis of renal lymphangiectasia. Four out of eight patients (50%) did not undergo aspiration of fluid and were offered conservative treatment. Two out of eight patients (25%) were donors for renal transplantation who were managed conservatively.
    Results: Renal lymphangiectasia was diagnosed on CT IVP. In each case, where aspiration of collection fluid was offered, the laboratory diagnosis of renal lymphangiectasia was confirmed and patients were managed conservatively. However, large collection in one patient was relieved by percutaneous aspiration.
    Conclusions: Renal lymphangiectasia can be diagnosed with CT scan and confirmed by laboratory tests. As it may be confused with other cystic lesions of kidney; proper diagnosis and exclusion of other differentials can be effectively offered by CT scan IVP, which can avoid unnecessary invasive treatment options.
    MeSH term(s) Adult ; Aged ; Contrast Media/administration & dosage ; Female ; Humans ; Iohexol/administration & dosage ; Kidney Diseases/diagnostic imaging ; Lymphangiectasis/diagnostic imaging ; Male ; Middle Aged ; Tomography, X-Ray Computed/methods ; Ultrasonography
    Chemical Substances Contrast Media ; Iohexol (4419T9MX03)
    Language English
    Publishing date 2017-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 632949-4
    ISSN 1525-6049 ; 0886-022X
    ISSN (online) 1525-6049
    ISSN 0886-022X
    DOI 10.1080/0886022X.2017.1337584
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 1331: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)

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  9. Article: Renal arteriovenous malformation presenting with massive hematuria.

    Gandhi, Shruti P / Patel, Kajal / Pandya, Vaidehi / Raval, Manish

    Radiology case reports

    2015  Volume 10, Issue 1, Page(s) 1068

    Abstract: Renal arteriovenous malformations are abnormal communications between the intrarenal arterial and venous systems. They are a rare cause of hematuria. Color Doppler ultrasonography, multislice CT angiography, and DSA are important tools for making the ... ...

    Abstract Renal arteriovenous malformations are abnormal communications between the intrarenal arterial and venous systems. They are a rare cause of hematuria. Color Doppler ultrasonography, multislice CT angiography, and DSA are important tools for making the diagnosis. We describe the case of a 62-year-old man with renal arteriovenous malformation who presented with gross hematuria.
    Language English
    Publishing date 2015-12-03
    Publishing country Netherlands
    Document type Case Reports
    ZDB-ID 2406300-9
    ISSN 1930-0433
    ISSN 1930-0433
    DOI 10.2484/rcr.v10i1.1068
    Database MEDical Literature Analysis and Retrieval System OnLINE

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