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    A child with glomangioma and osteochondroma on the same leg: A case report
    (2008) Köksal Y.; Çalişkan U.; Reisli I.; Uçar C.; Avunduk M.C.
    Glomangioma is a rare neoplasm that typically occurs in soft tissue of the extremities, particularly the subungual region of the fingertip. Osteochondromas are benign proliferations composed of mature bone and a cartilaginous cap. A case involving a 9-year-old boy with two benign masses (glomangioma and osteochondroma) on his right leg is presented. To our knowledge, this is the first case of glomangioma associated with osteochondroma in a child that has been reported.
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    Iatrogenic Vitamin D Intoxiciation in Infancy: Three Cases
    (2007) Ünal E.; Köksal Y.; Keleş S.; Artaç H.; Reisli İ.; Energin V. M.
    The potential hazards of excessive administration of vitamin D are well known. The increased intestinal absorption of calcium due to vitamin D over dosage leads to hypercalcemia and hypercalciuria that may give rise to the development of nephrocalcinosis, urolithiasis, and soft tissue calcification. Clinical features of three cases of iatrogenic vitamin D intoxication with different radiological findings were presented. The dose of vitamin D should be carefully determined in order to avoid vitamin D intoxication, and its complications. In addition, public health measures should be undertaken to prevent drug consumption without prescription that may be dangerous especially for children.
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    Our results lymphadenopathy biopsy in children: A review of the literature [Çocuklarda Lenfadenopati Biyopsi Sonuçlarimiz: Literatürün Gözden Geçirilmesi]
    (OrtadogŸu Reklam Tanitim Yayincilik Turizm Egitim Insaat Sanayi ve Ticaret A.S., 2016) Sekmenli T.; Çiftci I.; Köksal Y.
    Objective: Lymphadenopathy, is one of the most common presenting complaints in pediatricians routine. Parental concerns about the removal of the malignancy is a challenge for physicians. In our clinic, we aimed to evaluate retrospectively cases due to biopsy lymphadenopathy. Material and Methods: The medical records of the patients diagnosed with lymphadenopathy and underwent a biopsy between January 2011 and January 2014 in our clinic were examined retrospectively. The files of these patients were studied for the variables of age, gender, location, histopathology results, and symptoms. Results: 23 patients, 16 male and 7 female, had been conducted a diagnostic biopsy due to lymphadenopathy. The average age of the patients was 8.8 (1-17). Out of these 23 biopsies conducted, the histopathological findings in 10 patients suggested lymphadenitis, in 9 benignant lesions, and in 4 malignant lesions. Out of the 10 patients, diagnosed with lymphadenitis, 3 had chronic granulomatous lymphadenitis. Conclusion: Diagnosis can be sufficient most cases to be in detailed history and physical examination. Etiology in most cases is limited and a role in infections and benign structures such as nonspecific reactive hyperplasia. In order to clarify the etiology and and discard malignity in lymphadenopathies, a biopsy made according to the indication clears the path of the clinician. Copyright © 2016 by Tür ki ye Kli nik le ri.
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    Three Cases with Langerhans Cell Histiocytosis with Sistemic Involvement [Sistemik Tutulum ile Giden Langerhans Hücreli Histiositozis'li Üç Vaka Sunumu]
    (2004) Köksal Y.; Gülyüz A.; Çalişkan Ü.; Reisli I.; Uçar C.
    Histiocytosis which is a proliferative process characterized by an accumulation of dentritic cells in various tissues and organs is a rare disease. It can occur as an isolated lesion or as widespread systemic disease involving virtually any body site. Langerhans cell histiocytosis was diagnosed by light microscopy in a 27-month-old boy and 16-month-old girl with anemia hepatosplenomegaly, exanthema and lesions on the skull and a 9-month-old girl with thymic and cutaneous involvement. Clinical and laboratory findings of the cases are discussed in the light of literature.