Uncommon Causes of Thyrotoxicosis*
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Novel Application of Quantitative Single-Photon Emission Computed
Original Article | Nuclear Medicine https://doi.org/10.3348/kjr.2017.18.3.543 pISSN 1229-6929 · eISSN 2005-8330 Korean J Radiol 2017;18(3):543-550 Novel Application of Quantitative Single-Photon Emission Computed Tomography/Computed Tomography to Predict Early Response to Methimazole in Graves’ Disease Hyun Joo Kim, MD1, 2, Ji-In Bang, MD1, Ji-Young Kim, MD, PhD1, Jae Hoon Moon, MD, PhD3, Young So, MD, PhD4, Won Woo Lee, MD, PhD1, 5 Departments of 1Nuclear Medicine and 3Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea; 2Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Suwon 16229, Korea; 4Department of Nuclear Medicine, Konkuk University Medical Center, Seoul 05030, Korea; 5Institute of Radiation Medicine, Medical Research Center, Seoul National University, Seoul 08826, Korea Objective: Since Graves’ disease (GD) is resistant to antithyroid drugs (ATDs), an accurate quantitative thyroid function measurement is required for the prediction of early responses to ATD. Quantitative parameters derived from the novel technology, single-photon emission computed tomography/computed tomography (SPECT/CT), were investigated for the prediction of achievement of euthyroidism after methimazole (MMI) treatment in GD. Materials and Methods: A total of 36 GD patients (10 males, 26 females; mean age, 45.3 ± 13.8 years) were enrolled for this study, from April 2015 to January 2016. They underwent quantitative thyroid SPECT/CT 20 minutes post-injection of 99mTc- pertechnetate (5 mCi). Association between the time to biochemical euthyroidism after MMI treatment and %uptake, standardized uptake value (SUV), functional thyroid mass (SUVmean x thyroid volume) from the SPECT/CT, and clinical/ biochemical variables, were investigated. -
Thyroid Hormone Misuse and Abuse
Endocrine (2019) 66:79–86 https://doi.org/10.1007/s12020-019-02045-1 REVIEW Thyroid hormone misuse and abuse Victor J. Bernet 1,2 Received: 11 June 2019 / Accepted: 2 August 2019 © Springer Science+Business Media, LLC, part of Springer Nature 2019 Abstract Thyroid hormone (TH) plays an essential role in human physiology and maintenance of appropriate levels is important for good health. Unfortunately, there are instances in which TH is misused or abused. Such misuse may be intentional such as when individuals take thyroid hormone for unapproved indications like stimulation of weight loss or improved energy. There are instances where healthcare providers prescribe thyroid hormone for controversial or out of date uses and sometimes in supraphysiologic doses. Othertimes, unintentional exposure may occur through supplements or food that unknowingly contain TH. No matter the reason, exposure to exogenous forms of TH places the public at risk for potential adverse side effects. Keywords Thyrotoxicosis ● Thyroid hormone abuse ● Thyroid hormone misuse ● Factitious thyrotoxicosis ● Supplements ● 1234567890();,: 1234567890();,: Analogs Overdose Thyroid hormone misuse and abuse secondary to exogenous TH ingestion that may be unin- tentional or purposeful such as in some cases of Munch- Almost any substance that impacts body physiology and ausen syndrome. Instances of TH misuse can be associated function is at risk for misuse or frank abuse, usually in the with the development of significant side effects. There are misgiven belief that the particular agent whether it be a other instances of chronic, low-grade over treatment with herb, supplement, medication, or hormone has healing TH, which occur for various misreasoning such as weight properties beyond that of which it actually possesses. -
Thyroid Disease Update
10/11/2017 Thyroid Disease Update • Donald Eagerton M.D. Disclosures I have served as a clinical investigator and/or speakers bureau member for the following: Abbott, Astra Zenica, BMS, Boehringer Ingelheim, Eli Lilly, Merck, Novartis, Novo Nordisk, Pfizer, and Sanofi Aventis Thyroid Disease Update • Hypothyroidism • Hyperthyroidism • Thyroid Nodules • Thyroid Cancer 1 10/11/2017 2 10/11/2017 Case 1 • 50 year old white female is seen for follow up. Notices cold intolerance, dry skin, and some fatigue. Cholesterol is higher than prior visits. • Family history; Mother had history of hypothyroidism. Sister has hypothyroidism. • TSH = 14 (0.30- 3.3) Free T4 = 1.0 (0.95- 1.45) • Weight 70 kg Case 1 • Next step should be • A. Check Free T3 • B. Check AntiMicrosomal Antibodies • C. Start Levothyroxine 112 mcg daily • D. Start Armour Thyroid 30 mg q day • E. Check Thyroid Ultrasound Case 1 Next step should be • A. Check Free T3 • B. Check AntiMicrosomal Antibodies • C. Start Levothyroxine 112 mcg daily • D. Start Armour Thyroid 30 mg q day • E. Check Thyroid Ultrasound 3 10/11/2017 Hypothyroidism • Incidence 0.1- 2.0 % of the population • Subclinical hypothyroidism in 4-10% of the adult population • 5-8 times higher in women An FT4 test can confirm hypothyroidism 13 • In the presence of high TSH and FT4 levels in relation to the thyroid function TSH, low FT4 (free thyroxine) usually signalsTSH primary hypothyroidism12 Overt Mild Mild Overt Euthyroidism FT4 Hypothyroidism Thyrotoxicosis* Thyrotoxicosis vs. hyperthyroidism¹ While these terms are often used interchangeably, thyrotoxicosis (toxic thyroid), describes presence of too much thyroid hormone, whether caused by thyroid overproduction (hyperthyroidism); by leakage of thyroid hormone into the bloodstream (thyroiditis); or by taking too much thyroid hormone medication. -
Liothyronine Sodium(BANM, Rinnm) Potassium Perchlorate
2174 Thyroid and Antithyroid Drugs with methodological limitations. However, a controlled trial of In myxoedema coma liothyronine sodium may be liothyronine with paroxetine could not confirm any advantage of given intravenously in a dose of 5 to 20 micrograms by 3 O additive therapy. slow intravenous injection, repeated as necessary, usu- 1. Aronson R, et al. Triiodothyronine augmentation in the treat- HO I ally at intervals of 12 hours; the minimum interval be- ment of refractory depression: a meta-analysis. Arch Gen Psychi- OH atry 1996; 53: 842–8. tween doses is 4 hours. An alternative regimen advo- 2. Altshuler LL, et al. Does thyroid supplementation accelerate tri- NH2 cates an initial dose of 50 micrograms intravenously cyclic antidepressant response? A review and meta-analysis of I O the literature. Am J Psychiatry 2001; 158: 1617–22. followed by further injections of 25 micrograms every 3. Appelhof BC, et al. Triiodothyronine addition to paroxetine in I 8 hours until improvement occurs; the dosage may the treatment of major depressive disorder. J Clin Endocrinol then be reduced to 25 micrograms intravenously twice Metab 2004; 89: 6271–6. (liothyronine) daily. Obesity. Thyroid drugs have been tried in the treatment of obes- Liothyronine has also been given in the diagnosis of ity (p.2149) in euthyroid patients, but they produce only tempo- NOTE. The abbreviation T3 is often used for endogenous tri-io- hyperthyroidism in adults. Failure to suppress the up- rary weight loss, mainly of lean body-mass, and can produce se- dothyronine in medical and biochemical reports. Liotrix is USAN rious adverse effects, especially cardiac complications.1 for a mixture of liothyronine sodium with levothyroxine sodium. -
Salutary Lessons from TGA-Approved Sources for Thyroid-Related Medications
REVIEW Barriers in the quest for quality drug information: salutary lessons from TGA-approved sources for thyroid-related medications Jim R Stockigt n iodine-replete countries, about 5% of the population have a ABSTRACT thyroid disorder,1 of whom about a quarter will require long- • term medication either to correct deficiency or to control Product information (PI) for thyroid-related medications I endorsed by the Therapeutic Goods Administration, as thyroid hormone excess. In 2005, about 700 000 Pharmaceutical Benefits Scheme prescriptions were filled in Australia for thyrox- reproduced in the commonly used compilation publications ine, with about 80 000 scripts for the antithyroid drugs carbima- June 2006 MIMS (Monthly index of medical specialties) zole and propylthiouracil.2 annual, MIMS Online and the Australian prescription products Although no major new therapeutic agent has been introduced in guide 2006, was evaluated to see whether it reflects The Medical Journal of Australia ISSN: 0025- contemporary therapeutic practice. the thyroid729X 15 field January for 2007some 186 years, 2 76-79 the body of knowledge and • evidence©The has Medicaladvanced. Journal It is important of Australia that these 2007 developments are Compared with current medical literature, these PI-based reflectedwww.mja.com.au in the product information (PI) widely used by medical sources provide inadequate, inaccurate or outdated practitionersReview and a range of health professionals, who may not refer therapeutic directives. Examples include: directly to current scientific literature on thyroid disorders. MIMS ¾ Incorrect advice that thyroxine therapy should always 3 (Monthly index of medical specialties) annual, in its 30th edition in begin at very low dosage. -
Fate of Sodium Pertechnetate-Technetium-99M
JOURNAL OF NUCLEAR MEDICINE 8:50-59, 1967 Fate of Sodium Pertechnetate-Technetium-99m Dr. Muhammad Abdel Razzak, M.D.,1 Dr. Mahmoud Naguib, Ph.D.,2 and Dr. Mohamed El-Garhy, Ph.D.3 Cairo, Egypt Technetium-99m is a low-energy, short half-life iostope that has been recently introduced into clinical use. It is available as the daughter of °9Mowhich is re covered as a fission product or produced by neutron bombardement of molyb denum-98. The aim of the present work is to study the fate of sodium pertechnetate 9OmTc and to find out any difference in its distribution that might be caused by variation in the method of preparation of the parent nuclide, molybdenum-99. MATERIALS & METHODS The distribution of radioactive sodium pertechnetate milked from 99Mo that was obtained as a fission product (supplied by Isocommerz, D.D.R.) was studied in 36 white mice, weighing between 150 and 250 gm each. Normal isotonic saline was used for elution of the pertechnetate from the radionuclide generator. The experimental animals were divided into four equal groups depending on the route of administration of the radioactive material, whether intraperitoneal, in tramuscular, subcutaneous or oral. Every group was further subdivided into three equal subgroups, in order to study the effect of time on the distribution of the pertechnetate. Thus, the duration between administration of the radio-pharma ceutical and sacrificing the animals was fixed at 30, 60 and 120 minutes for the three subgroups respectively. Then the animals were dissected and the different organs taken out.Radioactivityin an accuratelyweighed specimen from each organ was estimated in a scintillation well detector equipped with one-inch sodium iodide thallium activated crystal. -
Package Insert TECHNETIUM Tc99m GENERATOR for the Production of Sodium Pertechnetate Tc99m Injection Diagnostic Radiopharmaceuti
NDA 17693/S-025 Page 3 Package Insert TECHNETIUM Tc99m GENERATOR For the Production of Sodium Pertechnetate Tc99m Injection Diagnostic Radiopharmaceutical For intravenous use only Rx ONLY DESCRIPTION The technetium Tc99m generator is prepared with fission-produced molybdenum Mo99 adsorbed on alumina in a lead-shielded column and provides a means for obtaining sterile pyrogen-free solutions of sodium pertechnetate Tc99m injection in sodium chloride. The eluate should be crystal clear. With a pH of 4.5-7.5, hydrochloric acid and/or sodium hydroxide may have been used for Mo99 solution pH adjustment. Over the life of the generator, each elution will provide a yield of > 80% of the theoretical amount of technetium Tc99m available from the molybdenum Mo99 on the generator column. Each eluate of the generator should not contain more than 0.0056 MBq (0.15 µCi) of molybdenum Mo99 per 37 MBq, (1 mCi) of technetium Tc99m per administered dose at the time of administration, and not more than 10 µg of aluminum per mL of the generator eluate, both of which must be determined by the user before administration. Since the eluate does not contain an antimicrobial agent, it should not be used after twelve hours from the time of generator elution. PHYSICAL CHARACTERISTICS Technetium Tc99m decays by an isomeric transition with a physical half-life of 6.02 hours. The principal photon that is useful for detection and imaging studies is listed in Table 1. Table 1. Principal Radiation Emission Data1 Radiation Mean %/Disintegration Mean Energy (keV) Gamma-2 89.07 140.5 1Kocher, David C., “Radioactive Decay Data Tables,” DOE/TIC-11026, p. -
Loss of Pertechnetate from the Human Thyroid
LOSS OF PERTECHNETATE FROM THE HUMAN THYROID J. G. Shimmins Regional Dept. of Clinical Physics and Bioengineering, Western Regional Hospital Board, Glasgow, Scotland R. McG. Harden and W. D. Alexander University Department of Medicine, Western Infirmary, Glasgow, Scotland The pertechnetate ion, like the iodide ion, is Magnascanner V (3,6) were started immediately trapped by the thyroid gland (1 ). Several authors after injection and were continued for 45 mm when have claimed that pertechnetate is not bound in the five scans had normally been completed. The scan thyroid (2) and that the gland behaves as a single speed was 100 cm/sec, and the line spacing was compartment (3) . However, the finding of organic 1 cm. Venous blood samples were taken at 2, 8, 15, binding of 9DmTcin rats (4,5) raises the question 30 and 45 mm. One gram perchlorate was given of whether some such binding may not occur in man. orally as a crushed powder in nine subjects 50 mm In this study we have investigated the binding of after the intravenous administration of pertechne pertechnetate in the human gland by measuring the tate. The same amount was given orally to the re rate of pertechnetate discharge from it after per maining four 3 hr after intravenous administra chlorate administration and have compared this rate tion of pertechnetate. Scans were carried out for an of discharge with the normal loss rate of pertechne additional 45 min after perchlorate administration, tate from the thyroid (3). If pertechnetate is Un and blood samples were taken at 2, 8, 15 and 45 bound, it should be possible to discharge it from min. -
A Case of Thyrotoxic Paralysis Caused by Consumption of Iodocaseine
Journal of Health and Social Sciences 2019; 4,2:277-282 CASE REPORT IN EMERGENCY MEDICINE A case of thyrotoxic paralysis caused by consumption of iodocaseine Antonio Villa1, Gabriella Nucera2 Affiliations: 1 M.D., Department of Emergency, ASST Monza, PO Desio, Monza, Italy 2 M.D., Department of Emergency Medicine, ASST Fatebenefratelli-Sacco, PO Fatebenefratelli, Milano, Italy Corresponding author: Dr Antonio Villa, ASST Monza, PO Desio. Via Fiuggi, 56 20159 Milan, Italy. E-mail: [email protected] Abstract Acute hypokalaemic paralysis is a rare but treatable cause of acute limb weakness. Thyrotoxic paralysis is an uncommon, potentially life-threatening endocrine emergency and it is a rare complication of hyperthyroidism. The most common causes of hyperthyroidism include Graves’ disease, multinodular goiters or solitary thyroid nodule, and iodine-induced thyrotoxicosis ( Jod-Basedow syndrome). Thyreotoxicosis factitia, which is caused by the excessive ingestion of exogenous thyroid hormone or iodine derivatives administration, has been rarely reported as a cause of thyrotoxic paralysis. We describe the case of a young Caucasian male with flaccid paralysis of all four limbs and severe hypokalaemia after inappropriate iodine derivatives (iodocasein) intake to show, in conclusion, how critical care physicians need to be aware of this rare but curable condition. KEY WORDS: Iodocaseine; hypokalaemia; thyrotoxic paralysis. 277 Journal of Health and Social Sciences 2019; 4,2:277-282 Riassunto La paralisi acuta ipokaliemica è una causa rara ma curabile di astenia acuta. La paralisi tireotossica è un'e- mergenza endocrina non comune e potenzialmente pericolosa per la vita ed è una rara complicanza dell'i- pertiroidismo. L'ipertiroidismo è causato prevalentemente dalla malattia di Graves, da gozzi singoli o multi- nodulari, e dalla malattia indotta da iodio ( Jod-Basedow). -
Germ Cell Tumors )
Systemicist Pathology.. Lecture # 13 Title : FGT 5 ( Germ Cell Tumors ) Done by: Dema Mhmd Khdier A man may die, nations may rise and fall…….But an idea lives on Teratoma :tumor contain fully developed tissues and organs, including hair, teeth, muscle, and bone. Germ Cell Tumors 1)Teratoma _ Immature teratoma _ Mature teratoma : ** Cystic (dermoid cyst) ** Solid ** Monodermal teratoma 2) Dysgerminoma 3) Yolk sac tumor 4) Choriocarcinoma 5) Embryonal carcinoma 6) Mixed germ cell tumors ~Teratoma _15% to 20% of ovarian tumors _ in the first two decades of life _ Young age ↑ incidence of malignancy _ > 90% are benign mature cystic teratomas. Benign Mature Cystic Teratomas (Dermoid Cysts ) _Most common ovarian tumors in childhood _90% are unilateral, more on the right. Complications: 1) In 1%, malignant transformation of one of the tissue elements, usually SCC. 2)10-15% undergo torsion due to long pedicle. Torsion: twisting around,,, may cause obstruction and abdominal pain Gross: _Multiloculated cyst filled with sebum & matted hair. _Teeth protruding from a nodular projection. _ Occasionally foci of bone and cartilage. Microscopic : _Mature tissues representing all three germ cell layers. _A cyst lined by epidermal type epithelium with adnexal appendages. Monodermal _Specialized _ teratoma _Usually solid and unilateral (one type of tissues ) *Struma ovarii _Composed of mature thyroid tissue. _ May produce hyperthyroidism. _Thyroid tumors may arise . *Ovarian carcinoid : Rarely produce carcinoid syndrome. ***Combined struma ovarii and carcinoid ~ Metastasis to Ovary Formation of fibrosis , 1)older ages 2) bilateral and multinodular 3) solid gray-white masses collagen around tumor 4)Malignant tumor cells arranged into cords and glands in a desmoplastic stroma cells 5) Cells may be "signet-ring" mucin-secreting 6) Primaries: GI (Krukenberg tumors), breast, lung. -
EANM Practice Guideline/SNMMI Procedure Standard for RAIU and Thyroid Scintigraphy
European Journal of Nuclear Medicine and Molecular Imaging (2019) 46:2514–2525 https://doi.org/10.1007/s00259-019-04472-8 GUIDELINES EANM practice guideline/SNMMI procedure standard for RAIU and thyroid scintigraphy Luca Giovanella 1,2 & Anca M. Avram3 & Ioannis Iakovou4 & Jennifer Kwak5 & Susan A. Lawson3 & Elizabeth Lulaj6 & Markus Luster7 & Arnoldo Piccardo8 & Matthias Schmidt9 & Mark Tulchinsky10 & Frederick A. Verburg7 & Ely Wolin11 Received: 11 July 2019 /Accepted: 29 July 2019 / Published online: 7 August 2019 # Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract Introduction Scintigraphic evaluation of the thyroid gland enables determination of the iodine-123 iodide or the 99mTc-pertechnetate uptake and distribution and remains the most accurate method for the diagnosis and quantification of thyroid autonomy and the detection of ectopic thyroid tissue. In addition, thyroid scintigraphy and radioiodine uptake test are useful to discriminate hyperthyroidism from destructive thyrotoxicosis and iodine-induced hyperthyroidism, respectively. Methods Several radiopharmaceuticals are available to help in differentiating benign from malignant cytologically indeterminate thyroid nodules and for supporting clinical decision-making. This joint practice guideline/procedure standard from the European Association of Nuclear Medicine (EANM) and the Society of Nuclear Medicine and Molecular Imaging (SNMMI) provides recommendations based on the available evidence in the literature. Conclusion The purpose of this practice guideline/procedure standard is to assist imaging specialists and clinicians in recommending, performing, and interpreting the results of thyroid scintigraphy (including positron emission tomography) with various radiopharmaceuticals and radioiodine uptake test in patients with different thyroid diseases. Keywords Thyroid . Scintigraphy . Radioiodine uptake test . 99mTc-sestaMIBI, 18F-fluorodeoxyglucose Preamble approval of the Committee on Guidelines and Board of Directors of both organizations. -
Hypothyroidism
Hypothyroidism Alejandro Diaz, MD,*† Elizabeth G. Lipman Diaz, PhD, CPNP‡ *Miami Children’s Hospital, Miami, FL †The Herbert Wertheim College of Medicine, Florida International University, Miami, FL ‡University of Miami School of Nursing and Health Studies, Miami, FL Educational Gap Congenital hypothyroidism is one the most common causes of preventable intellectual disability. Awareness that not all cases are detected by the newborn screening is important, particularly because early diagnosis and treatment are essential in preserving cognitive abilities. Objectives After completing this article, readers should be able to: 1. Identify the causes of congenital and acquired hypothyroidism in infants and children. 2. Interpret an abnormal newborn screening result and understand indications for further evaluation and treatment. 3. Recognize clinical signs and symptoms of hypothyroidism. 4. Understand the importance of early diagnosis and treatment of congenital hypothyroidism. 5. Understand the presentation, diagnostic process, treatment, and prognosis of Hashimoto thyroiditis. 6. Differentiate thyroid-binding globulin deficiency from central hypothyroidism. AUTHOR DISCLOSURE Drs Diaz and Lipman Diaz have disclosed no financial relationships 7. Identify sick euthyroid syndrome and other causes of abnormal thyroid relevant to this article. This commentary does function test results. not contain a discussion of an unapproved/ investigative use of a commercial product/ device. ABBREVIATIONS CH congenital hypothyroidism BACKGROUND FT3 free triiodothyronine FT4 free thyroxine The thyroid gland produces hormones that have important functions related to energy HT Hashimoto thyroiditis metabolism, control of body temperature, growth, bone development, and maturation LT4 levothyroxine of the central nervous system, among other metabolic processes throughout the body. rT3 reverse triiodothyronine The thyroid gland develops from the endodermal pharynx.