Search results

1

Venous malformation of epiglottis and arterio-venous malformation of palate treated by sclerotherapy – case reports

100%

Białaczewski L., Maciaszczyk K., Supeł M.

Polski Przegląd Otorynolaryngologiczny

|

2016

|

vol. 5(4)

29-35

EN

This study presents two rare clinical entities of vascular anomalies localized in the region of head and neck: the case of woman with venous malformation of the epiglottis and the man with the arterio-venous malformation of palate. Here in the title the term vascular malformation has been used because of conformity with the classification of International Society for the Study of Vascular Anomalies. Another, interchangeably used term hemangioma, defined according to Word Health Classification of Tumours, is more familiar in clinics. The foam sclerotherapy treatment has been reported with success. Microfoam prepared from polidocanol was injected directly into malformations. Large, ball-shaped laryngeal malformation decreased. In this case, sclerotherapy provides a good preparation for further surgery. Arteriovenous malformation of palate disappeared and there was no need for supplementary surgery. Authors did not observe any complications of the treatment.

2

Malformacja żylna nagłośni i malformacja tętniczo-żylna podniebienia leczone metodą skleroterapii – opis przypadków

100%

Białaczewski L., Maciaszczyk K., Supeł M.

Polski Przegląd Otorynolaryngologiczny

|

2016

|

vol. 5(4)

29-35

PL

W pracy przedstawiono dwa rzadkie przypadki anomalii naczyniowych w zakresie głowy i szyi: kobietę z malformacją żylną nagłośni i mężczyznę z malformacją tętniczo-żylną podniebienia. Użyte przez autorów w tytule pracy nazwy rozpoznań są zgodne z aktualną klasyfikacją kliniczną proponowaną przez Międzynarodowe Towarzystwo Badań nad Anomaliami Naczyniowymi (ISSVA). Według innej stosowanej przez patologów WHO klasyfikacji guzów naczyniowych, opisywana malformacja żylna to naczyniak jamisty, zaś malformacja tętniczo-żylna to naczyniak tętniczo-żylny. Pacjentów leczono metodą skleroterapii. Po wstrzyknięciach do malformacji polidokanolu w postaci piany stwierdzono regresję zmian. Duża, kulista malformacja nagłośni znacznie się zmniejszyła, umożliwiając jej wycięcie nożem elektrycznym, zaś malformacja podniebienia uległa całkowitemu zanikowi. Żadnych powikłań leczenia nie zaobserwowano.

3

Phenotypic evaluation of patients with Pendred syndrome

76%

Maciaszczyk K., Pniewska-Siark B., Gajewicz W., Stefańczyk L., Durko T., Pajor A., Lewiński A.

Otolaryngologia Polska

|

2008

|

vol. 62(6)

740-746

EN

Introduction. The Pendred syndrome (PS) is an autosomally recessively inherited disease. Its diagnosis requires identifi cation of the classical triad of symptoms, including hypoacusis, thyroid goitre and iodine organifi cation defect in the thyroid, which may lead to thyroid functional disorders of hypothyroidism. SP is accompanied by anatomical anomalies. The objective is the hearing and balance system evaluation and the analysis of the inner ear structure and also the assessment of the function and structure of thyroid gland. Material and methods. For the research four families were qualifi ed, 7 persons with PS, 12 persons altogether. In all the patients the anamnesis in the form of a questionnaire and laryngological examination were performed. It was followed by pure tone, speech and impedance audiometry and brainstem response testing as well. ENG was also conducted. Patients with hearing loss were subjected to magnetic resonance of temporal bone. For the whole group thyroid hormones levels and iodine organifi cation in the thyroid identifi ed in a test with potassium perchlorate were measured and also USG and scyntography were conducted. Results. In audiological examination in 3 cases deafness, in 2 cases profound hypoacusis and in 2 mild hypoacusis were recognised. In the group in 2 patients the hypoacusis was of a mixed type. In radiological assessment the labirynth showed anatomical anomalies in the form of enlargement of the vestibular aqueduct and the endolyphatic sac, yet in 3 patients the anomalies also concerned the structure of cochlear and semicircular canals. Endocrine examination showed hypothyroidism in 5, its subclinical form in 1, diffuse thyroid goitre in 4 and nodular thyroid goiter in 2 cases. Conclusions. A complex clinical evaluation: endocrine and audiological, together with radiological diagnostic imaging, supported by molecular studies of SLC26A4 gene, are the procedures, necessary for complete and accurate diagnosis of PS and EVAS.

4

Ocena fenotypowa pacjentów z zespołem Pendreda

76%

Maciaszczyk K., Pniewska-Siark B., Gajewicz W., Stefańczyk L., Durko T., Pajor A., Lewiński A.

Otolaryngologia Polska

|

2008

|

vol. 62(6)

740-746

PL

Introduction. The Pendred syndrome (PS) is an autosomally recessively inherited disease. Its diagnosis requires identifi cation of the classical triad of symptoms, including hypoacusis, thyroid goitre and iodine organifi cation defect in the thyroid, which may lead to thyroid functional disorders of hypothyroidism. SP is accompanied by anatomical anomalies. The objective is the hearing and balance system evaluation and the analysis of the inner ear structure and also the assessment of the function and structure of thyroid gland. Material and methods. For the research four families were qualifi ed, 7 persons with PS, 12 persons altogether. In all the patients the anamnesis in the form of a questionnaire and laryngological examination were performed. It was followed by pure tone, speech and impedance audiometry and brainstem response testing as well. ENG was also conducted. Patients with hearing loss were subjected to magnetic resonance of temporal bone. For the whole group thyroid hormones levels and iodine organifi cation in the thyroid identifi ed in a test with potassium perchlorate were measured and also USG and scyntography were conducted. Results. In audiological examination in 3 cases deafness, in 2 cases profound hypoacusis and in 2 mild hypoacusis were recognised. In the group in 2 patients the hypoacusis was of a mixed type. In radiological assessment the labirynth showed anatomical anomalies in the form of enlargement of the vestibular aqueduct and the endolyphatic sac, yet in 3 patients the anomalies also concerned the structure of cochlear and semicircular canals. Endocrine examination showed hypothyroidism in 5, its subclinical form in 1, diffuse thyroid goitre in 4 and nodular thyroid goiter in 2 cases. Conclusions. A complex clinical evaluation: endocrine and audiological, together with radiological diagnostic imaging, supported by molecular studies of SLC26A4 gene, are the procedures, necessary for complete and accurate diagnosis of PS and EVAS.

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2 Otolaryngologia Polska

2 Polski Przegląd Otorynolaryngologiczny

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4 Maciaszczyk K.

2 Białaczewski L.

2 Durko T.

2 Gajewicz W.

2 Lewiński A.

2 Pajor A.

2 Pniewska-Siark B.

2 Stefańczyk L.

2 Supeł M.

Venous malformation of epiglottis and arterio-venous malformation of palate treated by sclerotherapy – case reports

Malformacja żylna nagłośni i malformacja tętniczo-żylna podniebienia leczone metodą skleroterapii – opis przypadków

Phenotypic evaluation of patients with Pendred syndrome

Ocena fenotypowa pacjentów z zespołem Pendreda