F Kanadikirik

Publications (3)3.4 Total impact

• Article: Pelvic ganglioneuroma.

  K Guzin, S Afsar, A Yigit, S A Eren, E Ozerden, F Kanadikirik
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  ABSTRACT: Ganglioneuroma is a rare benign neurogenic tumor originating from the sempathoadrenal nervous system and is considered the benign counterpart of neuroblastoma, lacking the immature neuroblastic cells. A case of pelvic ganglioneuroma is described.
  International Journal of Gynecological Cancer 04/2008; 18(3):553-6. · 1.65 Impact Factor
• Article: Synchronous primary cancers of the endometrium and ovary: a case report.

  K Güzin, C Tekcan, M M Naki, S Kayataş, E Zemheri, F Kanadikirik, S Berkman
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  ABSTRACT: Synchronous primary cancers of the endometrium and ovary are found in 5% of women with endometrial cancer and 10% of women with ovarian cancer. In the present case, a multigravid 46-year-old woman complained of lower abdominal pain and abdominal distension. She did not define abnormal uterine bleeding. Screening ultrasound revealed a papillary containing structure, irregular, cystic 16 x 15 x 10 cm right ovarian mass. Preoperative endometrial biopsy revealed endometrioid adenocarcinoma. Ascites sampling, radical hysterectomy, bilateral salpingo-oophorectomy, pelvic and paraaortic lymphadenectomy, omentectomy, appendectomy and cytologic sampling of the undersurface of the diaphragm were carried out. Intraoperative and histological examinations showed Stage IIIC papillary serous carcinoma and stage IC endometrioid adenocarcinoma. Synchronous genital tract neoplasms constitute a more common clinical problem than would generally be expected.
  European journal of gynaecological oncology 02/2006; 27(4):425-8. · 0.47 Impact Factor
• Article: Short rib-polydactyly syndrome.

  M M Naki, D Gür, E Zemheri, C Tekcan, F Kanadikirik, R Has
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  ABSTRACT: Short rib-polydactyly syndrome (SRPD) is an autosomal recessive, lethal skeletal dysplasia. It is characterized by short limb dwarfism, short ribs with thoracic hypoplasia, polydactyly, and multiple anomalies of major organs. We report a case of SRPD subtype II (Majewski) that was detected in the 36th week of gestation, showing hydropic change, narrow thorax, shortened limbs, protuberant abdomen, micromelia, polydactyly and extremely low set ears, depressed nasal bridge, and cleft palate. The family was informed of the fatal outcome of the condition. Delivery was induced, and the baby died just after the birth. Prenatal diagnosis is established with postmortem radiographic and pathologic examinations.
  Archives of Gynecology and Obstetrics 08/2005; 272(2):173-5. · 1.28 Impact Factor