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  1. Article: Synchronous pancreas and gallbladder cancer with concomitant alopecia totalis.

    Kumar, Saket / Chandra, Abhijit

    Turkish journal of surgery

    2023  Volume 39, Issue 2, Page(s) 169–172

    Abstract: A 55-year-old female presented with history of pain in the right hypochondrium along with complete loss of facial and scalp hair over last two months. On evaluation, she was found to have locally advanced, synchronous malignancies of the gallbladder and ... ...

    Abstract A 55-year-old female presented with history of pain in the right hypochondrium along with complete loss of facial and scalp hair over last two months. On evaluation, she was found to have locally advanced, synchronous malignancies of the gallbladder and head of the pancreas. Synchronous malignancy of gallbladder and pancreas is in itself very rare and less than 10 such cases have been reported in the world literature. Alopecia totalis has been classically associated with various autoimmune disorders. However, alopecia totalis as a presenting feature of any abdominal malignancy has never been reported in the medical literature. The present report describes a rare association of synchronous pancreatobiliary malignancies with strange clinical presentation.
    Language English
    Publishing date 2023-06-19
    Publishing country Turkey
    Document type Case Reports
    ISSN 2564-6850
    ISSN 2564-6850
    DOI 10.47717/turkjsurg.2022.4457
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Comment On "GallBladder Duplication with Choledochal Cyst: A Rare Entity".

    Kumar, Saket / Singh, Ritu

    Journal of Indian Association of Pediatric Surgeons

    2023  Volume 28, Issue 6, Page(s) 549

    Language English
    Publishing date 2023-11-02
    Publishing country India
    Document type Journal Article
    ZDB-ID 2164528-0
    ISSN 1998-3891 ; 0971-9261
    ISSN (online) 1998-3891
    ISSN 0971-9261
    DOI 10.4103/jiaps.jiaps_159_23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Retroperitoneal dermoid cyst in a young boy.

    Kumar, Saket / Chidipotu, Venkat Rao

    The Pan African medical journal

    2021  Volume 38, Page(s) 36

    Language English
    Publishing date 2021-01-14
    Publishing country Uganda
    Document type Journal Article
    ZDB-ID 2514347-5
    ISSN 1937-8688 ; 1937-8688
    ISSN (online) 1937-8688
    ISSN 1937-8688
    DOI 10.11604/pamj.2021.38.36.27680
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: A rare case of black and white pancreas.

    Singla, Saurabh / Kumar, Saket

    Surgery

    2021  Volume 170, Issue 1, Page(s) e1–e2

    MeSH term(s) Abdominal Pain/etiology ; Female ; Humans ; Middle Aged ; Pancreas/diagnostic imaging ; Pancreatic Diseases/complications ; Pancreatic Diseases/diagnostic imaging
    Language English
    Publishing date 2021-03-15
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 202467-6
    ISSN 1532-7361 ; 0039-6060
    ISSN (online) 1532-7361
    ISSN 0039-6060
    DOI 10.1016/j.surg.2021.02.017
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    In stock of ZB MED Cologne/Königswinter

    Uk I Zs.129: Show issues Location:
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    bis Jg. 2021: Bestellungen von Artikeln über das Online-Bestellformular
    ab Jg. 2022: Lesesaal (EG)

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  5. Article ; Online: Giant stentolith: A rare complication of long-dwelling biliary endoprosthesis.

    Kumar, Saket / Chandra, Abhijit

    Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology

    2020  Volume 21, Issue 2, Page(s) 132–134

    Abstract: Endoscopic biliary stenting is performed for various indications in routine clinical practice. Plastic stents are indicated primarily for short-term biliary decompression and require removal or exchange after 12-16 weeks. However, patients who become ... ...

    Abstract Endoscopic biliary stenting is performed for various indications in routine clinical practice. Plastic stents are indicated primarily for short-term biliary decompression and require removal or exchange after 12-16 weeks. However, patients who become asymptomatic after the procedure may not return for scheduled stent removal and subsequently present with severe complications. We herein present the case of a 57-year-old female who underwent biliary stenting after the endoscopic clearance of bile duct stones. Her symptoms resolved after the intervention, but she was lost to follow-up with the stent remaining in situ. Four years later, she presented with pain in the right hypochondrium and experienced recurrent episodes of cholangitis. Magnetic resonance cholangiopancreatography revealed a retained plastic stent in the proximal bile duct with a large stone cast around the stent-a stentolith. Owing to the large stone size and proximal migration of the retained biliary stent, the patient required open surgical exploration for stentolith removal. Patients with forgotten biliary stents presenting with serious complications are not uncommon in India. Unaware of the complications of long-dwelling biliary stents, patients ignore the advice for the timely removal of biliary stents. Detailed patient counselling, education and documentation are essential to avoid this condition.
    MeSH term(s) Cholangiopancreatography, Magnetic Resonance/methods ; Cholangitis/etiology ; Cholangitis/physiopathology ; Cholangitis/surgery ; Cholelithiasis/surgery ; Decompression, Surgical/instrumentation ; Device Removal/methods ; Female ; Foreign Bodies/diagnostic imaging ; Foreign Bodies/etiology ; Foreign Bodies/physiopathology ; Foreign Bodies/surgery ; Humans ; Lost to Follow-Up ; Middle Aged ; Postoperative Period ; Sphincterotomy, Endoscopic/adverse effects ; Sphincterotomy, Endoscopic/instrumentation ; Sphincterotomy, Endoscopic/methods ; Stents/adverse effects ; Time-to-Treatment ; Treatment Outcome
    Language English
    Publishing date 2020-05-15
    Publishing country Egypt
    Document type Case Reports ; Journal Article
    ZDB-ID 2502114-X
    ISSN 2090-2387 ; 1687-1979
    ISSN (online) 2090-2387
    ISSN 1687-1979
    DOI 10.1016/j.ajg.2020.04.008
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  6. Article: Electrorheology and shear dependent reversible gelation of elongated α-FeOOH suspensions

    Kumar, Saket / Marapureddy, Sai Geetha / Thareja, Prachi

    Colloids and surfaces. 2021 July 20, v. 621

    2021  

    Abstract: We study the effect of applying an external electric field (E) on the rheology and microstructure of α-FeOOH, length (L) = 488 ± 20 nm and an aspect ratio of (5 ± 0.8) – in – silicone oil suspensions (α-FeOOH/silicone oil). The α-FeOOH/silicone oil ... ...

    Abstract We study the effect of applying an external electric field (E) on the rheology and microstructure of α-FeOOH, length (L) = 488 ± 20 nm and an aspect ratio of (5 ± 0.8) – in – silicone oil suspensions (α-FeOOH/silicone oil). The α-FeOOH/silicone oil suspensions show Newtonian response up to α-FeOOH particle volume fraction of 0.039 when no E is applied. The suspensions exhibit τy ~ E² and E¹.⁵ scaling in the low and high E regimes respectively and the normalized τy versus E data of the suspensions collapses onto single master curve, irrespective of the particle loading and applied E. The solid-like behavior of the suspensions is also evident from the frequency-independent storage modulus, and the plateau in relaxation modulus with applied E. The optical microscopy reveals the E driven irreversible network formation of α-FeOOH particles, which does not relax to a uniform dispersion of α-FeOOH particles when the E is switched off. The suspensions demonstrate a reversible ER response once they are sheared at constant shear rate of 10 s⁻¹.
    Keywords electric field ; gelation ; light microscopy ; microstructure ; oils ; rheology ; silicone ; storage modulus
    Language English
    Dates of publication 2021-0720
    Publishing place Elsevier B.V.
    Document type Article
    Note NAL-AP-2-clean
    ZDB-ID 1500517-3
    ISSN 0927-7757
    ISSN 0927-7757
    DOI 10.1016/j.colsurfa.2021.126579
    Database NAL-Catalogue (AGRICOLA)

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  7. Article: Aggressive Inflammatory Myofibroblastic Tumor of Distal Pancreas: A Diagnostic and Surgical Challenge.

    A G, Harisankar / Kumar, Saket / Singla, Saurabh / Kurian, Nishant

    Cureus

    2022  Volume 14, Issue 3, Page(s) e22820

    Abstract: An inflammatory myofibroblastic tumor (IMT) is a rare soft tissue neoplasm of unknown etiology. It is a slow-growing tumor of borderline malignant potential. Distant metastases and recurrence after complete excision are rare. Establishing a preoperative ... ...

    Abstract An inflammatory myofibroblastic tumor (IMT) is a rare soft tissue neoplasm of unknown etiology. It is a slow-growing tumor of borderline malignant potential. Distant metastases and recurrence after complete excision are rare. Establishing a preoperative diagnosis is difficult because of its nonspecific clinic-radiological features. Although the majority of cases have been reported in the lungs, it can affect any part of the body. The pancreatic inflammatory myofibroblastic tumor is very rare and only 26 cases have been reported in the medical literature. These tumors mostly arise from the head of the pancreas, whereas occurrence in the body or tail region is rather unusual. Here, we report a case of a 55-year-old male patient with a locally advanced inflammatory myofibroblastic tumor arising from the pancreatic tail. Complete excision of tumor required multi-visceral resection (distal pancreaticosplenectomy with jejunal and colonic segmental resection). The diagnosis of inflammatory myofibroblast tumor was made on the basis of histopathology and immunohistochemistry.
    Language English
    Publishing date 2022-03-03
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2747273-5
    ISSN 2168-8184
    ISSN 2168-8184
    DOI 10.7759/cureus.22820
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  8. Article ; Online: Minimally invasive approach to Herlyn-Werner-Wunderlich syndrome with giant endometriotic cyst: a case report.

    Kumar, Saket / Dayal, Madhukar / Kumar, Abhay / Singh, Nidhi / Singh, Vijay Prakash

    The Pan African medical journal

    2023  Volume 44, Page(s) 79

    Abstract: Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly of the Mullerian and Wolffian ductal system, manifesting as a triad of dipelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis. Patients usually remain asymptomatic till ... ...

    Abstract Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly of the Mullerian and Wolffian ductal system, manifesting as a triad of dipelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis. Patients usually remain asymptomatic till menarche and experience progressive dysmenorrhea, suprapubic lump, and/or features of infection (pyometra, pelvic collection, etc.) afterward. We hereby present a case of a young lady with Herlyn-Werner-Wunderlich syndrome with a large endometriotic cyst, likely arising from the right hemiuterus. She presented with dysmenorrhea and progressive abdominal distention for seven years. She was treated by laparoscopic ovarian cyst excision and right hemihysterectomy that relieved her symptoms.
    MeSH term(s) Humans ; Female ; Dysmenorrhea/etiology ; Endometriosis/complications ; Endometriosis/diagnosis ; Endometriosis/surgery ; Uterus/surgery ; Menarche ; Kidney Diseases/diagnosis ; Kidney Diseases/surgery
    Language English
    Publishing date 2023-02-08
    Publishing country Uganda
    Document type Case Reports
    ZDB-ID 2514347-5
    ISSN 1937-8688 ; 1937-8688
    ISSN (online) 1937-8688
    ISSN 1937-8688
    DOI 10.11604/pamj.2023.44.79.32667
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Laparoscopic management of an ileal lipoma presenting with massive gastrointestinal haemorrhage.

    Kumar, Saket / Harisankar, A G / Kumar, Pankaj / Kumar, Abhay / Parween, Rana

    Journal of minimal access surgery

    2023  

    Abstract: Small bowel lipomas are benign submucosal neoplasm composed mainly of mature adipose tissue. Despite their rare occurrence, lipomas are the second most common benign tumour of the small intestine. These tumours are mostly small in size and remain ... ...

    Abstract Small bowel lipomas are benign submucosal neoplasm composed mainly of mature adipose tissue. Despite their rare occurrence, lipomas are the second most common benign tumour of the small intestine. These tumours are mostly small in size and remain clinically asymptomatic. However, larger lesions tend to be more symptomatic, presenting with complications such as intussusception, bleeding or obstruction. Definitive surgical or endoscopic intervention is indicated in such symptomatic lipomas. Herein, we describe a rare case of ileal lipoma presenting with ileo-ileal intussusception and a life-threatening haemorrhage that was managed by laparoscopic-assisted ileal resection.
    Language English
    Publishing date 2023-03-14
    Publishing country India
    Document type Journal Article
    ZDB-ID 2186884-0
    ISSN 1998-3921 ; 0972-9941
    ISSN (online) 1998-3921
    ISSN 0972-9941
    DOI 10.4103/jmas.jmas_152_22
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Bardet-Biedl Syndrome with Choledochal Cyst: Rare Association with a Novel Variant.

    Kumar, Saket / Harisankar, A G / Singh, Nidhi / Kumar, Singh Rakesh / Mayank, Nilay

    Journal of Indian Association of Pediatric Surgeons

    2023  Volume 28, Issue 6, Page(s) 520–522

    Abstract: Bardet-Biedl syndrome is an autosomal-recessive ciliopathic disorder affecting multiple organ systems. Characteristic features include progressive retinal dystrophy, obesity, polydactyly hypogonadism, mental retardation, and renal disorders. Other ... ...

    Abstract Bardet-Biedl syndrome is an autosomal-recessive ciliopathic disorder affecting multiple organ systems. Characteristic features include progressive retinal dystrophy, obesity, polydactyly hypogonadism, mental retardation, and renal disorders. Other manifestations include congenital heart diseases, hepatic fibrosis, ataxia, and diabetes. Approximately 30% of patients with Biedl-Bardet syndrome (BBS) have hepatobiliary disorders such as periportal fibrosis, nonalcoholic fatty liver disease, and cystic dilation of the bile ducts. The association of BBS with choledochal cysts (CDC) is extremely rare. Here, we report a case of a 14-year-old boy with a novel variant of BBS and associated type IV CDC. The patient was managed surgically with CDC excision and Roux-en-Y hepaticojejunostomy.
    Language English
    Publishing date 2023-11-02
    Publishing country India
    Document type Case Reports
    ZDB-ID 2164528-0
    ISSN 1998-3891 ; 0971-9261
    ISSN (online) 1998-3891
    ISSN 0971-9261
    DOI 10.4103/jiaps.jiaps_124_23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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