Isil Bulur’s research while affiliated with Eskişehir Osmangazi University and other places

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Publications (3)


Table 5 : Photosensitive drugs most commonly used by the patients 
The efficacy and safety of phototherapy in geriatric patients: A retrospective study
  • Article
  • Full-text available

February 2018

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180 Reads

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18 Citations

Anais Brasileiros de Dermatologia

Isil Bulur

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Background While phototherapy is a well-established treatment for many dermatoses, data from the literature regarding its use in elderly patients are quite limited. Objective In this study, we aimed to determine the phototherapy indications in geriatric patients and to evaluate the effectiveness and reliability of phototherapy in this group. Methods This study included 95 patients of 65 years of age and older who were treated in our phototherapy unit between 2006 and 2015. The data for this study were collected retrospectively from patient follow-up forms in the phototherapy unit. Results Phototherapy was administered to 28 (29.5%) patients for mycosis fungoides, 25 (26.3%) patients foplaque type psoriasis, 12 (12.6%) patients for palmoplantar psoriasis, 12 (12.6%) patients for generalized pruritus, and 18 (19%) for other dermatoses. Of the patients, 64.2% had received a narrowband UVB (NB-UVB), 21.1% oral psoralen UVA (PUVA), and 14.7% local PUVA treatment. A complete response was achieved in 76.9-85.7% of the mycosis fungoides and in 73.71-100% of the psoriasis vulgaris patients treated with NB-UVB and PUVA, respectively. All the patients with generalized pruritus were treated with NB-UVB, and 80% of these patients achieved significant improvement. The erythema rate was found to be 0.43% per session for NB-UVB treatment and 0.46% per session for PUVA treatment as a side effect. Study limitations The limitations of our study are that it was retrospective and the remission durations of the patients are not known. Conclusion This study showed that phototherapy is effective and reliable in the elderly population with proper dose increases and close follow-up.

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Table 1 . Characteristics of 53 patients with morphea 
Morphea in Middle Anatolia, Turkey: A 5-year single-center experience

August 2017

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68 Reads

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9 Citations

Introduction Morphea, also referred to as localized scleroderma, is a rare fibrosing skin disorder of undetermined cause. Aim We report our single-center experience with morphea. Material and methods The study included 53 patients who were diagnosed with morphea by histopathology in our department between 2010 and 2015. Study data were collected retrospectively from the records of morphea patients. Results The study included 53 patients (38 women, 15 men), and median age at onset was 39.0 (range: 8–85) years. Thirty (56.6%) patients had circumscribed morphea, 15 (28.3%) had generalized morphea, and 7 (13.2%) had linear morphea. One patient had mixed variant morphea (generalized, pansclerotic and linear morphea). ANA positivity was detected in 12 (22.6%) patients, but analysis for an association between the presence of ANA and morphea types, patients’ characteristics did not reveal any significant associations. We did not observe any extracutaneous manifestations in patients during follow-up period. There were 2 of 53 patients who had concomitant autoimmune disorder including vitiligo and spondyloarthritis. Thirty (56.6%) patients received only topical treatment. The patients with clinical improvement who were treated with systemic therapy received methotrexate (26.4%), colchicine (9.4%), mycophenolate mofetil (5.7%) and prednisolone (1.9%). Conclusions Our results related to the demographic data of the patients and morphea types were consistent with the literature. On the other hand we observed that methotrexate was mostly used as an effective treatment option for generalized morphea.


Citations (3)


... Few treatment options have been proposed for hDPs, but they have not been proven effective owing to the limitations of the different study designs [13]. For pruritic diseases, several protocol dosages of NB-UVB were used according to disease or centers considering their effectiveness and side effects [14]. in 1977, >400 mJ/cm 2 was found to relieve pruritic symptoms in hDPs [15]; however, low-dose NB-UVB did not show a significant reducing effect on pruritus intensity unlike the control group, which showed such effect on refractory uremic pruritus [16,17]. in 2009, nalfurafine hydrochloride was reported to effectively reduce itchiness that was otherwise refractory to the currently available treatments for patients receiving maintenance hDPs, with few significant adverse drug reactions [11]. another agent, difelikefalin, was studied and found to effectively reduce itching intensity and improve sleep-and itch-related quality of life [18]. ...

Reference:

Comparison of effect and mechanism between nalfurafine hydrochloride and narrow-band ultraviolet B phototherapy in the treatment of pruritus in hemodialysis patients
The efficacy and safety of phototherapy in geriatric patients: A retrospective study

Anais Brasileiros de Dermatologia

... Other clinical assessments for disease activity were more formal and did include specific criteria that was utilized to categorize patients. For example, one study [14] evaluated defined clinical improvement in activity as the absence of the criteria suggested by Careta and Romiti: appearance of new lesions in the last 3 months, expansion of the pre-existing lesion in the last 3 months, moderate or severe erythema or skin lesions with erythematous borders, violaceous lesion or lesion border, increased induration of the lesion border, and worsening of the hair loss on the scalp, eyebrows or eyelashes. Other clinical assessments described in the articles included the evaluation of surgical outcomes or general clinician satisfaction/success by assessing facial symmetry, complications, and need for surgical revisions. ...

Morphea in Middle Anatolia, Turkey: A 5-year single-center experience

... The samples taken were inoculated on SDA (Sabouraud Dextrose Agar, MERCK), SDA-CCG (Sabouraud Dextrose Agar with Cycloheximide-chloramphenicol-gentamicin, MERCK) and MA (Mycobiotic agar, MERCK) media and kept in an incubator at 22-26 °C; inoculation was done on SDA, SDA-CCG media and incubated at 37 °C for 4 weeks [21]. During the incubation, it was checked every two days to see if there was any growth, and those that did reproduce were processed for identification. ...

The Identification of an Uncommon Dermatophyte as an Agent of Tinea Corporis, Microsporum Ferrugineum / Tinea Corporis’in Nadir Bir Etkeni Olarak Microsporum Ferrugineum’un İdentifikasyonu
  • Citing Article
  • July 2017

OSMANGAZİ JOURNAL OF MEDICINE