ACTA ENDOCRINOLOGICA (BUC)

The International Journal of Romanian Society of Endocrinology / Registered in 1938

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Year Volume Issue First page
10.4183/aeb.
Author
Title
Abstract/Title
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  • Case Report

    Stanescu B, Miron R, Badiu C

    Anaplastic carcinoma of the thyroid mimicking acute thyroiditis

    Acta Endo (Buc) 2007 3(4): 493-502 doi: 10.4183/aeb.2007.493

    Abstract
    We report a case of anaplastic thyroid carcinoma mimicking acute thyroiditis with skin necrosis. A 82 years woman, with no significant previous medical disorders, was admitted with a few weeks history of a painful rapidly enlarging neck mass associated with hoarseness, dysphagia to solids, dyspnea and a general state deterioration. Physical exam was significant for a left-anterior lateral neck tumor of about 7 cm. The mass was tender, firm, nonpulsatile and nonfluctuant; it was fixed to the underlying cervical tissues. Antero-cervical skin tissues were swollen, hyperemic, presenting necrosis with penetrating tendency, severe neck pain and tenderness, associated with fever, suggesting an acute thyroiditis. The thyroid function was normal (TSH = 0.81 mUI/L, TT3 = 62 ng/dL, TT4= 8.77 ug/dL) as well as antithyroid peroxidase antibody (0.5 UI/mL), while thyreoglobulin was high (384 ng/mL). Thyroid scintigram revealed a cold nodule. Thyroid ultrasound revealed a giant left thyroid mass with necrosis, lymph nodes involvement and displacement of trachea. Fine needle aspiration confirmed the clinical suspicion features of anaplastic thyroid cancer: mitoses, anisocytosis and marked anisokaryosis with enlarged nuclei. Computed tomography confirmed a voluminous mass involving the thyroid, with calcifications, necrosis with multiple latero-cervical lymph nodes, compressing right carotid artery and internal jugular vein; it was detected also a pulmonary metastasis (right medium pulmonary lobe). The patient was diagnosed on having a thyroid carcinoma of the anaplastic type, TNM stage IVc. Surgery was performed through cervical approach without sternotomy, by total thyroidectomy and resection of proximal cervical structures involved by the tumor mass. After surgery, the patient was started on levothyroxine 100 μg/ day and scheduled for cervical radiotherapy, but the tumor relapsed in several weeks. Local disease can be controlled with radiotherapy either alone or in combination with chemotherapy.
  • Book Review

    Badiu C

    Harrison's Principles of Internal Medicine 16th ed

    Acta Endo (Buc) 2005 1(4): 499-499 doi: 10.4183/aeb.2005.499

  • Book Review

    Badiu C

    Textbook of Nephro-Endocrinology: 2nd Edition

    Acta Endo (Buc) 2017 13(4): 523-523 doi: 10.4183/aeb.2017.523

  • Notes & Comments

    Enciu O, Toma EA, Badiu C, Miron A

    A Close Encounter – Left Pneumonia and Pancreatic Tail Fistula after Laparoscopic Left Adrenalectomy

    Acta Endo (Buc) 2020 16(4): 526-529 doi: 10.4183/aeb.2020.526

    Abstract
    Laparoscopic adrenalectomy is currently considered the gold standard for adrenal tumors up to 6 cm, and although with far less morbidity than the open alternative, when it comes to its complications we should not look away. The case concerns a 51-year old obese male that underwent left laparoscopic adrenalectomy for incidentaloma and developed pancreatic tail fistula. Without an evident pancreatic lesion during surgery and an uneventful early postoperative course the patient was discharged only to return 4 days later with respiratory symptoms and mild abdominal discomfort in the left upper quadrant. The CT scan diagnosed a left subphrenic fluid collection and left basal pneumonia, thus the patient underwent laparoscopic reintervention for drainage of the pancreatic fluid collection and received conventional antibiotherapy for pneumonia. The patient was discharged in good condition with the drainage tube in situ. The drainage tube was extracted 14 days later.
  • Book Review

    Badiu C

    ENDOCRINE SELF-ASSESSMENT PROGRAM ESAP 2021 QUESTIONS, ANSWERS, DISCUSSIONS

    Acta Endo (Buc) 2020 16(4): 535-535 doi: 10.4183/aeb.2020.535

  • Images in Endocrinology

    Lider S, Gheorghiu M, Milos I, Badiu C

    Malignant Paraganglioma Non-Responsive to MIBGIn MEN2A Syndrome

    Acta Endo (Buc) 2022 18(4): 536-537 doi: 10.4183/aeb.2022.536

  • Actualities in medicine

    Dobrescu R, Badiu C

    An Expanding Class in the Treatment of Thyroid Cancer: Tyrosine Kinase Inhibitors

    Acta Endo (Buc) 2015 11(4): 536-539 doi: 10.4183/aeb.2015.536

    Abstract
    Thyroid cancer, the most frequent endocrine malignancy, is in most patients a treatable disease, with excellent outcome and cure rate. However, a few patients present with rapidly progressive metastatic differentiated thyroid cancer which loses the radioiodine uptake capacity. These rare cases are prone to a rapid evolution and poor prognosis. Medullary thyroid cancer is a neuroendocrine tumor occurring sporadically or as part of endocrine tumor syndromes, genetic tests being part of standard clinical evaluation. Current knowledge of tumor biology in thyroid cancer allowed development of a new class of drugs, thyrosine kinase inhibitors (TKI). Their use in clinical trials allowed the development of more specific drugs, increasingly effective and with less adverse reactions, interfering with multiple thyrosine kinase enzymes. Improvement of the progression free survival, decrease of tumor volume and tumor markers, as well as patients with stable disease on TKI are strong arguments for including patients in clinical trials. Currently, only four TKI are approved by FDA: sorafenib and lenvatinib for DTC; vandetanib and cabozantinib for MTC. In this paper we present this new class of drugs used in the treatment of aggressive thyroid cancer.
  • Book Review

    Badiu C

    Health Equity in Endocrinology

    Acta Endo (Buc) 2023 19(4): 538-538 doi: 10.4183/aeb.2023.538

  • Images in Endocrinology

    Badiu C, Dobrescu M, Ginghina C

    When pericardiotomy becomes compulsory!

    Acta Endo (Buc) 2010 6(4): 539-539 doi: 10.4183/aeb.2010.539

  • Images in Endocrinology

    Dobrescu M, Verzea S, Badiu C

    Infarct-like features induced by pheochromocytoma

    Acta Endo (Buc) 2009 5(4): 543-543 doi: 10.4183/aeb.2009.543