Yazar "Canda, Serefettin" seçeneğine göre listele

Listeleniyor 1 - 3 / 3
  • Küçük Resim
    Öğe
    Granular Cell Tumor of the Posterior Tibial Nerve as a Rare Cause of Heel Pain A Case Report
    (Amer Podiatric Med Assoc, 2009) Dogramaci, Yunus; Kalacı, Aydıner; Sevinc, Teoman Toni; Hakverdi, Sibel; Canda, Serefettin; Yanat, Ahmet Nedim
    Granular cell tumor of peripheral nerves is extremely rare. We present the case of a patient with a well-capsulated intraneural granular cell tumor involving the posterior tibial nerve, who presented with chronic heel pain mimicking plantar fasciitis. Magnetic resonance imaging revealed a well-defined intraneural soft-tissue mass within the substance of the posterior tibial nerve. Histopathologic examination showed a granular cell tumor, which is extremley rare in the peripheral nerves. Heel pain is one of the common conditions handled by physicians, podiatrists, and orthopedic surgeons. Posterior tibial nerve lesions at the leg should be kept in mind in the differential diagnosis of patients with persistent heel and foot pain. Magnetic resonance imaging is a useful method in the anatomical evaluation of focal intraneural lesions. (J Am Podiatr Med Assoc 99(3): 254-257, 2009)
  • Küçük Resim
    Öğe
    Pediatric Cutaneous Mastocytosis: Demographic, Clinical and Histopathological Findings
    (Galenos Yayincilik, 2008) Serarslan, Gamze; Atik, Esin; Canda, Serefettin
    Objective: Mastocytosis is a disease characterized by abnormal growth and accumulation of mast cells in one or more organ systems. The skin is the most commonly affected organ. It is aimed to present demographic, clinical and histopathological findings of pediatric patients with cutaneous mastocytosis and a review of the literature in this study. Methods: Demographic, clinical and histopathological data of 14 pediatric patients with cutaneous mastocytosis were retrospectively analyzed. Results: Eleven patients (78.6%) had urticaria pigmentosa, two patients (14.3%) had mastocytoma and one patient (% 7.1) had coexistence of both urticaria pigmentosa and mastocytoma. The onset of the disease occured in the first year of life in 64.3% of patients. Male-female ratio was 1:1.8. Lesions were localised most commonly on the trunk and extremities in patients with urticaria pigmentosa and on the trunk in patients with mastocytoma. Darier's sign was present in 92% of patients. There was one patient with a positive family history. The most frequent complaint was pruritus. Conclusion: Generally our resuls, except for the predominance of girls, are compatible with the studies given earlier.
  • Küçük Resim
    Öğe
    Periosteal Chondroma of the Ischium; An Unusual Location
    (De Gruyter Open Ltd, 2012) Akansu, Bulent; Atik, Esin; Altintas, Suleyman; Kalacı, Aydıner; Canda, Serefettin
    Periosteal chondroma is a rare benign tumor of hyaline cartilage. Periosteal chondroma arising in the ischium is an extremely rare event. By presenting this case report, we aim to remind that differential diagnosis of these lesions should be carefully performed especially for unusual locations. A 51-year-old man visited the orthopedics clinic with the complaints of left pelvic mass and pain lasting about one year. Computed tomography showed a solid mass with abundant specks of calcification that was 4x5 cm in diameter and associated with the ischium of the left pelvic bone. There was no evidence of penetration into the medullary cavity and cortical sclerosis. No radiological aggressive appearance was observed. The lesion was removed with the covering periosteum. Microscopically, there were lobules of hyaline cartilage composed of chondrocytes with foci of endochondral ossification and calcification. The case was reported as 'periosteal' chondroma'. In conclusion, this case report presents a case of periosteal chondroma, a rare tumor, which occurred in an unusual location and age range. The differential diagnosis of periosteal chondroma from malignant lesions is necessary for avoiding aggressive and inappropriate treatment.