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  1. Article ; Online: Hurthle cell tumours of the thyroid. Personal experience and review of the literature.

    Barnabei, A / Ferretti, E / Baldelli, R / Procaccini, A / Spriano, G / Appetecchia, M

    Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale

    2010  Volume 29, Issue 6, Page(s) 305–311

    Abstract: ... by Hurthle cell tumour that may predict disease progression and death. In the literature, factors potentially associated ... the Authors identified 28 patients affected by Hurthle cell tumour, 9 with Hurthle cell adenoma and 19 ... Hurthle cell carcinoma represents about 5% of differentiated thyroid carcinomas. The prognosis ...

    Abstract Hurthle cell carcinoma represents about 5% of differentiated thyroid carcinomas. The prognosis of the malignant type of the tumour is still under debate as some Authors have reported that Hurthle cell adenoma occasionally behaves like Hurthle cell carcinoma. Aim of the present study was to evaluate previously reported data and personal experience on the clinical and pathological features of patients affected by Hurthle cell tumour that may predict disease progression and death. In the literature, factors potentially associated with decreased survival were identified and include: age, disease stage, tumour size, extra-glandular invasion, lymph node disease, distant metastases, extensive surgery, radioiodine treatment. From 1992 to 2003, the Authors identified 28 patients affected by Hurthle cell tumour, 9 with Hurthle cell adenoma and 19 with Hurthle cell carcinoma. Of these, 22 were females and 6 males. Mean age of patients affected by adenoma was 49.7 years (range 30-72) vs. 49.3 years (range 15-72) in Hurthle cell carcinoma patients. In all patients, total thyroidectomy was performed. At histology, 9 adenomas, 5 "minimally invasive" and 14 invasive carcinomas were found. Post-operatively, in Hurthle cell carcinoma patients, TNM staging showed 9 patients with stage I, 5 stage II, 4 stage III and one stage IVa (UICC, 2002). All invasive carcinomas underwent (131)I therapy (91-585 mCi). One Hurthle cell carcinoma patient received external beam radiotherapy. The mean follow-up period was 62 months (range 6-324). Relapse was not observed in any of the cases with adenoma. Only one Hurthle cell carcinoma patient showed distant lung metastases at 60 months' follow-up. In conclusion, Hurthle cell carcinoma was not found to present a more aggressive behaviour than follicular carcinoma, when risk factors, including extent of tumour invasion, were taken into account. None of the patients with Hurthle cell adenoma showed a relapse or death caused by the tumour.
    MeSH term(s) Adenoma, Oxyphilic ; Adult ; Aged ; Female ; Humans ; Male ; Middle Aged ; Prognosis ; Retrospective Studies ; Thyroid Neoplasms/diagnosis
    Language English
    Publishing date 2010-04-08
    Publishing country Italy
    Document type Journal Article ; Review
    ZDB-ID 604898-5
    ISSN 1827-675X ; 0392-100X
    ISSN (online) 1827-675X
    ISSN 0392-100X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Hürthle cell tumors of the thyroid gland. Personal experience and review of literature.

    Bononi, Marco / De Cesare, Alessandro / Cangemi, Vincenzo / Fiori, Enrico / Galati, Gaspare / Giovagnoli, Maria Rosaria / Izzo, Luciano / Cimitan, Andrea / Meucci, Massimo / Cavallaro, Antonino

    Anticancer research

    2002  Volume 22, Issue 6B, Page(s) 3579–3582

    Abstract: ... Discussion: Hürthle cell tumors can be diversified in adenoma and carcinoma. Almost all reports classify ... Background: Oncocytic cell neoplasm of the thyroid is currently recognized as a histological ... methods: The authors report six cases of Hürthle cell tumor. Five cases were adenoma, one was carcinoma ...

    Abstract Background: Oncocytic cell neoplasm of the thyroid is currently recognized as a histological entity, but doubts still exist about its clinical and evolutionary categorization. Controversies concern occurrence and frequency of malignant forms, natural history and therapeutic strategies.
    Materials and methods: The authors report six cases of Hürthle cell tumor. Five cases were adenoma, one was carcinoma. Morpho-functional pre-operative evaluation and inter-operative histopathological test were performed in all patients. One patient underwent lobectomy (absence of unusual characteristics of the adenoma Hürthle cell) and five underwent total thyroidectomies (1 carcinoma). All patients were treated with suppressive hormonal therapy.
    Results: No mortality and morbidity was recorded. All patients are undergoing follow-up (adenomas: average 64.2 months; carcinoma: 132 months) and none of them show recurrent symptoms.
    Discussion: Hürthle cell tumors can be diversified in adenoma and carcinoma. Almost all reports classify oncocytic nodules as malignant when capsular and/or vascular invasion is present or when there is peri-thyroid tissue infiltration or lymphatic or hematic metastases. A clear differentiation between adenoma and carcinoma is determined by a histological test. Also an intra-operative histopathological analysis is sometimes unable to show minimal signs of invasion. Conflicting observations about the biological behaviour of Hürthle cell neoplasm lead to different therapeutic strategies. The authors believe lobectomy is the treatment of choice when a clear histological diagnosis of adenoma has been made. When carcinoma is diagnosed or when doubts exist after intraoperative histological test, the authors recommend total thyroidectomy followed by scintigraphic test and preventive radio-active therapy. All patients should be treated with suppressive hormonal therapy and undergo periodic check-ups.
    MeSH term(s) Adenoma, Oxyphilic/pathology ; Adenoma, Oxyphilic/surgery ; Adult ; Female ; Humans ; Male ; Middle Aged ; Thyroid Neoplasms/pathology ; Thyroid Neoplasms/surgery
    Language English
    Publishing date 2002-11
    Publishing country Greece
    Document type Journal Article ; Review
    ZDB-ID 604549-2
    ISSN 1791-7530 ; 0250-7005
    ISSN (online) 1791-7530
    ISSN 0250-7005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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