Biomedical subjects

Zdenka Kuchynková

Publications and source records attributed to Zdenka Kuchynková.

3 recordsLinked to original sources

PubMed2003

Thyroid abscess at an adolescent age.

We report a case of thyroid abscess in a 17-year-old girl. She was presented with swelling and pain in the region of the left thyroid lobe. The diagnosis was confirmed by ultrasonography and fine needle aspiration. After incision, evacuation of the pus and antibiotic treatment manifestations of disease disappeared. Barium swallow did not prove any hypopharyngeal fistula. The girl is now without any problems for 3 years. The patient had infectious mononucleosis 2 months prior development of the thyroid abscess. We contemplate that it may had changed the immunological state that facilitated this rare inflammation.

Abscess↗

PubMed2000

CASE REPORT: Invasive fibrous thyroiditis (Riedel's disease) with signs of giant cell arteritis.

OBJECTIVES: The authors described a case of Riedel's thyroiditis, a relatively rare disease affecting the thyroid gland. RESULTS: A 38-year-old female was diagnosed with Riedel's thyroiditis by a frozen section examination during attempted surgery for the suspicion of malignancy. The histopathologic examination confirmed the diagnosis of Riedel's thyroiditis combined with signs of giant cell arteritis. After hemithyroidectomy, the patient had paresis of the recurrent laryngeal nerve for five days and signs of hypothyroidism and hypoparathyroidism for three months after surgery. The level of thyroid peroxidase antibodies titer was higher. The patient had no compression symptoms, no signs of systemic immunopathology, and no signs of extracervical fibrosis. She was put on prednison 5 mg daily. CONCLUSIONS: Riedel's thyroiditis can be looked upon as a cervical fibrosis of unknown etiology affecting the thyroid. In our case it was combined with signs of giant cell arteritis.

Journal Article↗

PubMed2000

Hemangiosarcoma of the Thyroid Gland. A case report.

OBJECTIVES: The authors described a case of rare histological type of primary thyroid tumor-angiosarcoma. Angiosarcoma generally represents a rare connective tissue tumor in the head and neck region. Its biological behavior is locally aggressive and destructive with a high recurrence rate. METHODS: A case of a rare histological type of primary thyroid tumor -angiosarcoma-has been described including fine needle aspiration biopsy, histology, and autopsy. RESULTS: Irrespective of the complex approach the angiosarcoma of the patient referred to was diagnosed in a radically inoperative stage of the disease. Radiation was therefore applied after the tumor mass was diminished with the partial thyroidectomy and a correct histopathological diagnosis was rendered. Nevertheless, the locally destructive course was followed with a rather rapid spread of the tumor (lymph nodes, bones, lungs, and brain). Autopsy proved with certainty that the thyroid was the primary tumor location. A suspected kidney origin due to an uncertain sonography shadow of this region was excluded with a complete absence of any neoplastic spread of the angiosarcoma in the abdominal cavity at all.

Journal Article↗