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  • 1
    Online Resource
    Online Resource
    S. Karger AG ; 2006
    In:  Pediatric Neurosurgery Vol. 42, No. 6 ( 2006), p. 395-398
    In: Pediatric Neurosurgery, S. Karger AG, Vol. 42, No. 6 ( 2006), p. 395-398
    Abstract: Iatrogenic spinal epidermoid tumors are extremely rare and may be caused by skin fragments which were implanted in the spine as a result of a trauma or lumbar puncture. Due to the time lag between the lumbar puncture and the development of a symptomatic tumor, this relationship is often overlooked and can cause a delay in the proper diagnosis. Here, we report a rare case of an intraspinal epidermoid tumor, which developed 7 years after a lumbar puncture in a 12-year-old boy, who presented with back pain and radiating pain to the posterior of both thighs. A total excision of the tumor via L 〈 sub 〉 3 〈 /sub 〉 –L 〈 sub 〉 4 〈 /sub 〉 hemilaminectomy yielded a good functional recovery.
    Type of Medium: Online Resource
    ISSN: 1016-2291 , 1423-0305
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2006
    detail.hit.zdb_id: 1483546-0
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  • 2
    In: Pediatric Neurosurgery, S. Karger AG, Vol. 42, No. 5 ( 2006), p. 304-307
    Abstract: Involvement of the cervical spinal cord by a solitary osteochondroma is rare. We describe a case of cervical osteochondroma extending from C5 to C7 in a 16-year-old male. The tumor, arising from the inner aspect of the C6 spinous process, projected longitudinally into the spinal canal and compressed the spinal cord; this caused clinical symptoms associated with myelopathy and radiculopathy. Total excision of the tumor by C5–C7 hemilaminectomy resulted in a good functional recovery.
    Type of Medium: Online Resource
    ISSN: 1016-2291 , 1423-0305
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2006
    detail.hit.zdb_id: 1483546-0
    Location Call Number Limitation Availability
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  • 3
    In: Dermatology, S. Karger AG, Vol. 237, No. 3 ( 2021), p. 330-337
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 Emerging data suggest that inflammatory bowel disease (IBD) and psoriasis are associated, sharing common genetic predispositions and immunological mechanisms. However, concrete data on psoriasis risk in IBD patients compared to the general population are limited. 〈 b 〉 〈 i 〉 Objective: 〈 /i 〉 〈 /b 〉 We investigated the risk of developing psoriasis in IBD patients compared to controls without IBD. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 Using the Korean National Health Insurance Database, patients diagnosed with Crohn’s disease (CD) or ulcerative colitis (UC) between 2005 and 2008 were age- and sex-matched 1:4 to non-IBD subjects from 2003 to 2018. IBD patients were defined by combining the International Classification of Diseases 10th revision code and at least one prescription of IBD-specific medications. Disease phenotypes, including psoriasis severity and psoriatic arthritis, were also identified. We investigated newly diagnosed psoriasis from 2009 to 2018. Incidence rates and risk of psoriasis were assessed with multivariate Cox regression models. Subgroup analyses for age and sex, and sensitivity analysis involving tumor necrosis factor (TNF) inhibitor-naïve patients were performed. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 During nearly a decade of follow-up, 20,152 IBD patients were identified (14,619 [72.54%] UC and 5,533 [27.46%] CD). Among them, 439 patients were newly diagnosed with psoriasis (incidence rate of 217.68 per 100,000 person-years and 228.62 per 100,000 person-years for UC and CD, respectively). The psoriasis risk was higher in IBD patients than in the matched controls (adjusted hazard ratio, aHR, 2.95, 95% confidence interval, CI, 2.60–3.33). Moreover, IBD patients aged & #x3c;30 years were at an increased risk (aHR 3.35, 95% CI 2.58–4.35), a trend that was unchanged across all psoriasis phenotypes. Sensitivity analysis of TNF inhibitor-naïve patients revealed consistent results. 〈 b 〉 〈 i 〉 Conclusions: 〈 /i 〉 〈 /b 〉 IBD patients were more likely to develop psoriasis compared to non-IBD subjects, including younger patients at an elevated risk regardless of TNF inhibitor use. This advocates the interplay between IBD and psoriasis; thus, inspection of cutaneous manifestation and dermatological consultation may be helpful in IBD patients at risk.
    Type of Medium: Online Resource
    ISSN: 1018-8665 , 1421-9832
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2021
    detail.hit.zdb_id: 1482189-8
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  • 4
    Online Resource
    Online Resource
    S. Karger AG ; 2022
    In:  Dermatology Vol. 238, No. 3 ( 2022), p. 571-578
    In: Dermatology, S. Karger AG, Vol. 238, No. 3 ( 2022), p. 571-578
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 The fecal immunochemistry test (FIT) has been proposed as a surrogate marker of intestinal inflammation. Psoriasis is a chronic inflammatory skin disease that is linked to underlying systemic inflammatory conditions, including inflammatory bowel disease. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 We investigated the association between occult blood in feces and the risk of psoriasis using data from the National Health Insurance System. This study was conducted involving 1,395,147 individuals who underwent health examinations from January 2009 to December 2012 and were followed up until the end of 2017. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 The incidence of psoriasis (per 1,000 person-years) was 3.76 versus 4.14 (FIT-negative versus FIT-positive group) during a median follow-up of 6.68 years. In the multivariable-adjusted model, the hazard ratios for psoriasis were 1.03 for one positive FIT result, 1.12 for two positive FIT results, and 1.34 for three positive FIT results compared with negative FIT results. 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 The risk of psoriasis was significantly increased in patients with positive FIT results compared to the FIT-negative population.
    Type of Medium: Online Resource
    ISSN: 1018-8665 , 1421-9832
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2022
    detail.hit.zdb_id: 1482189-8
    Location Call Number Limitation Availability
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