(AACE) Abbreviations, 4–6 Absorbed Radiation, 6, 199–200, 208, 3

Total Page:16

File Type:pdf, Size:1020Kb

(AACE) Abbreviations, 4–6 Absorbed Radiation, 6, 199–200, 208, 3 Index A prognosis of, 329–330 AACE. See American Association of Clinical prophylaxis for, 330 Endocrinologists (AACE) radiation and, 224 Abbreviations, 4–6 radiation complications and, 328 Absorbed radiation, 6, 199–200, 208, 315. See also symptoms of, 324 Radiation treatment of, 326–329 cumulative activity of, 207 radiation for, 327–328 Acne, 141 radioiodine and, 329 Acupuncture, 15 summary of, 329 Adenoma, 116 surgery for, 327 follicular, 65–66, 76, 85, 111 Anaplastic transformation, 322 paraganglioma-like, 65–66 Anesthetic. See General anesthetic; Local anesthetic Adenomatoid goiter. See Hyperplastic colloid Angiosarcoma, 85–86 nodule Antithyroglobulin antibodies, 192 Adenomatous hyperplasia, 62–65 Aplastic anemia, 148 AGES, 167, 201, 225 ATA. See American Thyroid Association formula for, 166 Autonomous nodule, 116, 154. See also Plummer’s Albumin, 36 disease Alternative therapy, 14–15 percutaneous injection of ethanol into, 119 American Association of Clinical Endocrinologists thyrotoxicosis and, treatment of, 116–117 (AACE), 13 American Thyroid Association (ATA), 13 B AMES, 166–167, 201 Baby. See also Fetus Amiodarone, 180 cancer in, 313, 317 Anaplastic carcinoma, 4, 79–80, 85, 88, 111, 143, 154, hypothyroidism and, 316 240, 248, 321–335 intelligence level of, 313, 317 chemotherapy and, 328 radiation exposure to, 308–309 children and, 296 B cell lymphoma, 84–85 clinical features of, 323 Benign tumor. See Nodule definition of, 79 Bleeding, 171 diagnosis of, 324 Bovine TSH, 175 etiology of, 321–323 Breast cancer, 238, 378–379, 381–382 experimental approaches to, 330–331 children and, 296 insular carcinoma and, 257 131I and, 221 131I therapy for, 222, 330 multimodality treatments for, 328–329 C pathology of, 323 Calcitonin, 49–50, 57, 60, 78, 81–82, 86, 151, 342–343, patient characteristics and, 323 346, 354, 357 385 386 Index Calcitonin (cont.) 123I treatment in, 291 elevated levels of, 352 Levo-thyroxine and, 289 measurement of, 345 limited workup in, 286 cAMP. See Cyclic AMP lobectomy in, 286 Cancer seeking radiopharmaceuticals, 105–106 low iodine diet for, 291 Carcinoma, 1. See also Anaplastic carcinoma; lymph node metastases in, 287, 298 Insular carcinoma; Papillary carcinoma myelogenous leukemia in, 297 c-cell origin of, 80–82 NIS in, 287–288 embolization of, 244–245 nodules in, 109–110, 285–287 mucoepidermoid, 84 papillary carcinoma in, 287, 297 poorly differentiated, 78, 255 PET scan in, 295–297 primary squamous cell, 86 postoperative complications with, 289 retinoic acid and, 246 postoperative scans in, 293 word usage, 6 postoperative timeline with, 290 Carcinoma showing thymus-like element (CASTLE), prepubertal, 2 83 radiation and, 291 CAT scan. See CT scan radioiodine treatment for, 289–297 C cell, 87–88, 337–338, 341, 348, 357. See also controversies of, 296–297 Parafollicular cell RET proto-oncogene in, 347 hyperplasia and, 347–348 scintiscan of, 285 Cervical lymph node, 108 Sistrunk procedure in, 287 Chemotherapy, 197–198, 331, 370 stunning of, 291, 296 anaplastic carcinoma and, 328 thymus and, 295 medullary carcinoma and, 348–351 thyroglobulin and, 293, 296–297 Chernobyl reactor accident, 76, 97, 135–136, 145, thyroglossal cyst in, 287 157, 255 thyroid cancer etiology in, 284 adult incidence of thyroid cancer from, 146 thyroid cancer in, 283–302 children and, 284 incidence of, 284 papillary carcinoma from, 76, 146, 153–154 long-term management of, 294 quantities of radionuclides released from, 145 pathology of, 287–288 Chest scan, 190–191 rhTSH treatment for, 292–293 Children surgery for, 288–289 anaplastic carcinoma and, 296 treatment of, 288, 290–291 cancerous nodule in, 124 thyroidectomy in, 283, 286, 289, 297–298, 347 Chernobyl reactor accident and, 284 thyroid hormone and, 289–290 Cowden’s syndrome in, 296 thyroid nodule in, 297 differentiated thyroid cancer prognosis in, 297 diagnosis of, 285–287 external radiation in, 284 misdiagnosis of, 285 false positive scans in, 294 presentation of, 285–287 FNA in, 285–287, 297 thyroxine and, 290 follicular carcinoma in, 287 TSH and, 289 Gardner’s syndrome in, 296 ultrasound and, 293 hemithyroidectomy in, 288–289 Chronic lymphocytic thyroiditis. See Hashimoto’s Hodgkin’s disease in, 297 thyroiditis hypoparathyroidism in, 289 Cochran’s heterogeneity statistic (Q), 12 hypothyroidism in, 284 Coherent scatter, 150 131I treatment in, 283, 286, 289–290, 293, 298 Collimator, 188, 191 breast cancer after, 296 Colloid, 32–35, 50, 59, 62, 64 complications and long term problems with, nodule, 63–65, 96, 115 294–296 Comet tail, 107 dosage of, 291–292 Compton scatter, 149–151 fertility in, 294–295 Computed tomographic scan. See CT scan management after, 293–294 Confidence intervals, 8–9 nausea in, 294 equation for, 8 offspring of, 296 Core biopsy, 109 pregnancy testing prior to, 296 Cowden’s syndrome, 155, 261 reduced sperm count in, 295 children and, 296 stunning by, 291, 296 Cranial nerve XI, 28 Index 387 CT (computed tomographic) scan, 139, 157, 164, Endocrine gland, 21, 49 179, 184, 205, 238, 241–243, 257, 260, 344, Endocytosis, 35 350, 368–369, 380 Equilibrium-absorbed dose constant, 207–208 PET scan and, 239 Estrogen, 32, 36, 195, 303 sensitivity of, 238 thyroid cancer and, 157 Cumulative activity, 207 Ethanol, 122, 124 Cyclic AMP, 28–29, 45 intracystic injection of, 120 Cyst, 96, 106, 247 intranodular injection of, 119 causes of, 70 side effects of, 119 determination of, sensitivity and specificity of, Euthyroid, 98–100, 101, 116–117, 121, 180, 210–211, 69 253 midline, 70 pregnancy and, 308, 316 Cystic lesions, 70 Evidence-based medicine, 10–11 Cystic nodule, 110 basis of, 12 definition of, 10 D External clinical evidence, 10 Death rate, 2 Degrees of freedom (df), 12 F Deiodinase, 36–37, 39–40 False positive findings, 185–191 Depression Familial differentiated thyroid carcinoma, 154, 164, hypothyroidism and, 175 261–262 thyroid cancer and, 175 prognosis of, 261 De Quervain’s thyroiditis, 324. See also Subacute Familial medullary carcinoma, 80, 88, 97, 135, 152, thyroiditis 155, 337, 339, 347, 356–357 Diagnostic accuracy, 111–113 categories of, 15 Diagnostic scanning, 173–181, 236–237 mutations associated with, 341 hypothyroidism and, 173–175 Familial non-medullary carcinoma. See Familial 124I and, 209 differentiated thyroid carcinoma postoperative timeline, 174 Familial tumors, 81 preparation for, 173 Family history, 97 rhTSH and, 211 Fetal thyroid, 314 timing of, 231–232 Fetus. See also Baby Dialysis, 223–224 absorbed radiation in, 315 Diet, low iodine, 178–180, 231, 237, 257, 262 hypothyroidism in, 312–313 children and, 291 radiation and, 312–316 hypothyroidism and, 179 followup testing for, 313 new mothers and, 309 legal ramifications of, 315, 317 Differentiated thyroid cancer, 3, 155, 163–282, 225, Fine needle aspiration (FNA), 25, 58, 60, 63, 65, 68, 248, 261, 322, 331 79, 86–87, 96, 101, 105–113, 116, 124, 172, child’s prognosis for, 297 238, 240, 247, 249, 252, 256–258, 261, 285, controversy management concerning, 225 324, 342–343, 346, 349, 357–358, 365, 368, definition of, 163 371–372, 377, 380, 382 ectopic location of, 246–254 benign diagnosis from, 110 familial, 164, 261–262 children and, 285–287, 297 natural history of, 164–165 guided, 112–113, 120, 352 presentation of, 163–164 interpretation of, 110–111 prognoses of, 165 papillary carcinoma and, 72 variants of, 4, 74, 163, 262 pregnancy and, 305–306, 316 Dosimetry, 199, 202, 206–211, 221, 223 problems with, 111 badges for, 214 repeat of, 114 diagnostic 124I using, 209 sensitivity and specificity of, 111 Non-excessive marrow, lung and total body techniques for, 108–110 radiation and, 209–210 Follicle, 49, 59, 64 structure of, 28 E Follicle stimulating hormone (FSH), 175, 222 Empiric therapy for ablation of remnants, 201–204 Follicular adenoma, 65–66, 76, 85, 111 Empiric therapy for metastases treatment, definition of, 65 204–206 uncommon variants of, 66 388 Index Follicular carcinoma, 3, 74, 76–78, 88, 100, 111, 114, Hashimoto’s thyroiditis, 68, 78, 84, 98, 101, 147, 192, 156, 163–164, 205, 244, 248, 251 240, 258, 365–366, 368, 371 children and, 287 primary thyroid lymphoma and, 367 familial, 154 HCG. See Human chorionic gonadotropin insular carcinoma and, 257 Hematolymphoid neoplasms, 84–85 metastatic, 164, 252 Hematoma, 262 poorly differentiated, 78–79 formation of, 109 variants of, 88, 258–261 postoperative occurrance of, 171 Follicular cell, 29–30, 33–35, 57, 62, 87–88, 173, 262, Hodgkin’s lymphoma, 85, 135, 136, 240 284, 321 children and, 297 Follicular lesions, 65 Hormone. See Thyroid, hormones of Free-3,5,3¢,5¢ tetraiodothyronine, 5 Horner’s syndrome, 27–28 FSH. See Follicle stimulating hormone Human apical iodide transporter, 33 FT4, 4, 196, 210, 305 Human chorionic gonadotropin (HCG), 175, 304, 314 index formula for, 303 Hürthle cell carcinoma, 63, 65, 68, 78, 81, 88, 104, 111, 154, 205, 240, 248, 255, 258–261, 262, G 321, 324 Gallium-67 (67Ga), 105, 148, 368 clinical features of, 259 Gardner’s syndrome, 155 diagnosis of, 259 children and, 296 familial, 155 Gastrointestinal tract, 29 papillary carcinoma and, 76 General anesthetic, 240 patient characteristics of, 259 inherent risks of, 172 prognosis of, 260 Genetic engineering, 50 summary of, 260 Glucose, 238–239 thyroid carcinoma and, 260–261 Goiter, 23, 29–30, 46, 104, 122, 124, 247, 304–305, 331, treatment of, 259–260 365, 371 Hürthle cell neoplasm, 258–259 asymptomatic, 121 Hyalinizing trabecular, 65–66, 83 causes of, 62 Hydrogen peroxide, 35 multinodular, 23, 76, 86, 102–104, 107, 125, 155, Hyperparathyroidism, 337, 343, 357 322, 378 Hyperplastic
Recommended publications
  • Volume 93 Number 2
    2014 - 2015 VOLUME 93, NUMBER 2 TABLE OF CONTENTS Journal of the PHILIPPINE MEDICAL ASSOCIATION 2014 - 2015 VOLUME 93, NUMBER 1 THE MYSTERY OF SALIVARY GLAND TUMORS 1 Kathleen M. Rodriguez, M.D., Celso V. Ureta, M.D., FPSOHNS, FPCS INFLAMMATORY CONDITION OF THE LARYNX VERSUS A 11 NEOPLASTIC LARYGEAL MASS: A DIAGNOSTIC DILEMMA Jeffrey A. Pangilinan, M.D, Celso V. Ureta, M.D., FPSOHNS, FPCS A CASE OF ACTINOMYCETOMA TREATED WITH CO-TRIMOXAZOLE 22 (TRIMETHOPRIM + SULFAMETHOXAZOLE) Subekcha Karki, M.D., Ma. Luisa Abad-Venida, M.D. EVALUATION OF SUPRACRICOID PARTIAL LANGECTOMY WITH 30 CRICOHYOIDOEPIGLOTTOPEXY IN A TERTIARY HOSPITAL Kathleen M. Rodriquez, M.D., Jeffrey A. Pangilinan, M.D. Celso V. Ureta, M.D., FPSOHNS, FPCS MIDLINE NECK FISTULA: 4TH BRANCHIAL CLEFT FISTULA vs. 48 INFECTED THYROGLOSSAL CYST Kathleen M. Rodriquez, M.D., Celso V. Ureta, M.D., FPSOHNS, FPCS LARGE ERYTHEMATOUS MASS OF THE AURICLE IN A 17-YEAR OLD 61 MALE: AN UNCOMMON PRESENTATION OF ACTURE MYELOGENOUS LEUKEMIA Eleanor P. Bernas, M.D., Natividad Almazan, M.D., FPSOHNS, FPCS Celso V. Ureta, M.D., FPSOHNS, FPCS A RARE CASE OF PARATHYROID CARCINOMA MANIFESTING AS 71 RECURRENT NEPHROLITHIASIS Ma. Melizza S. Villalon, M.D., Celso V. Ureta, M.D., FPSOHNS, FPCS REHABILITATION OF A DIGITAL VIDEOSTROBOSCOPY SYSTEM: 84 A PRACTICAL SOLUTION TO AN INOPERABLE AND UNSERVICEABLE DIGITAL VIDEOSTROBOSCOPY UNIT Jeffrey A. Pangilinan, M.D., Celso V. Ureta, M.D., FPSOHNS, FPCS RANDOMIZED DOUBLE BLIND PLACEBO-CONTROLLED CLINICAL 101 ON THE EFFICACY AND SAFETY OF MORINGA OLEIFERA (MALUNGGAY) 1% CREAM IN THE TREATMENT OF TINEA CORPORIS: A PILOT STUDY Charo Fionna F.
    [Show full text]
  • ICD-9-CM to ICD-10 Common Codes for Endocrinology
    Diagnostic Services ICD-9-CM to ICD-10 Common Codes for Endocrinology ICD-9 ICD-10 ICD-9 ICD-10 Diagnoses Diagnoses Code Code Code Code Adrenal Disorders 253.9 Pituitary lesions E23.7 Galactorrhea, not associated with 227.0 Pheochromocytoma of adrenal D35.00 611.6 N64.3 childbirth 255.0 Cushing’s syndrome E24.9 Thyroid Disorders 255.10 Aldosteronism E26.9 193 Thyroid cancer C73 255.10 Primary aldosteronism E26.09 240.0 Simple nontoxic goiter E04.0 Glucocorticoid-remediable 255.11 E26.02 aldosteronism 241.0 Nontoxic uninodular goiter E04.1 255.12 Conn’s syndrome E26.01 241.0 Thyroid nodule E04.1 255.13 Bartter’s syndrome E26.81 241.1 Nontoxic multinodular goiter E04.2 255.14 Secondary aldosteronism E26.1 242.00 Graves’ disease E05.00 255.2 Adrenal virilism E25.9 242.00 Primary thyroid hyperplasia E05.00 255.2 Adrenogenital disorder E25.9 242.00 Toxic diffuse goiter E05.00 255.2 Congenital adrenal hyperplasia E25.0 242.01 Graves’ disease with thyrotoxic crisis E05.01 Uninodular goiter - Thyrotoxic crisis 255.41 Addison’s disease E27.1 242.10 E05.10 (Hyperthyroidism) 255.41 Adrenal insufficiency E27.40 242.80 Drug induced hyperthyroidism E05.80 255.41 Glucocorticoid insufficiency E27.40 242.90 Hyperthyroidism E05.90 255.42 Hypoaldosteronism E27.40 242.91 Hyperthyroidism with thyrotoxic crisis E05.91 255.42 Mineralcorticoid deficiency E27.49 243 Congenital hypothyroidism E03.1 Carbohydrate Metabolism Disorders 244.0 Postsurgical hypothyroidism E89.0 251.0 Hypoglycemic coma E15 Hypothyroidism, secondary to 244.8 E03.8 251.2 Hypoglycemia E16.2
    [Show full text]
  • Surgery Team
    Common Neck Swellings With all courtesy to our colleagues, Raslan and his team, a lot of our work is based on their Manual to Surgery Booklet. Important Mentioned by doctors but not in slides Additional notes from Surgical Recall 6th edition or Raslan's booklet Not mentioned by the doctor 431 SURGERY TEAM Done By: Revised By: Fatema Sara Almutairi Abdulkarim Leaders Abeer Al-Suwailem Mohammed Alshammari Surgery Team 431 Primary hyperparathyroidism (Surgical Approach): There is a problem in diagnosis and management of primary hyperthyroidism in KSA, and in 3rd world countries in general. What are parathyroids? General characteristics: We have four parathyroid glands in the posterior aspect of the thyroid gland. They are very small corn-size, yellow with brownish and pinkish color glands. Both the superior and the inferior parathyroid glands receive blood supply from the inferior thyroid artery. Embryology of The parathyroid glands: The upper parathyroid glands originate from the 4th pharyngeal pouch. The lower parathyroid glands originate from the 3rd pharyngeal pouch. Physiology of the Parathyroid: Ca2+ homeostasis: release of Parathormone/Parathyroid hormone (PTH) to raise Ca2+ levels in the blood (PTH is not responsible of the levels of calcium in bones only in the serum). Whenever the serum calcium goes down, immediately PTH will be secreted from the parathyroids to calcium in the serum. Vitamin D regulation: PTH induces Vit.D hydroxylation in the kidney,and this process is necessary for Vit.D activation. Calcitonin: is released from the c-cells of the thyroid gland decrease Ca2+ levels. These are not of physiological significance. Parathermone hormone (PTH) affects three systems: 1) Direct affect on bones to get the calcium into the serum.
    [Show full text]
  • ICD-10-CM Codes for Endocrinology
    Diagnostic Services ICD-10-CM Codes for Endocrinology ICD 10 ICD 10 Diagnoses Diagnoses Code Code Adrenal Disorders E23.7 Pituitary lesions D35.00 Pheochromocytoma of adrenal N64.3 Galactorrhea, not associated with childbirth E24.9 Cushing’s syndrome Thyroid Disorders E25.0 Congenital adrenal hyperplasia C73 Thyroid cancer E25.9 Adrenal virilism E03.1 Congenital hypothyroidism E25.9 Adrenogenital disorder E03.8 Hypothyroidism, secondary to pituitary disease E26.01 Conn’s syndrome E03.9 Primary hypothyroidism E26.02 Glucocorticoid-remediable aldosteronism E04.0 Simple nontoxic goiter E26.09 Primary aldosteronism E04.1 Nontoxic uninodular goiter E26.1 Secondary aldosteronism E04.1 Thyroid nodule E26.81 Bartter’s syndrome E04.2 Nontoxic multinodular goiter E26.9 Aldosteronism E05.00 Graves’ disease E27.1 Addison’s disease E05.00 Primary thyroid hyperplasia E27.40 Adrenal insufficiency E05.00 Toxic diffuse goiter E27.40 Glucocorticoid insufficiency E05.01 Graves’ disease with thyrotoxic crisis E27.40 Hypoaldosteronism E05.10 Uninodular goiter - Thyrotoxic crisis (Hyperthyroidism) E27.49 Mineralcorticoid deficiency E05.80 Drug induced hyperthyroidism Carbohydrate Metabolism Disorders E05.90 Hyperthyroidism E15 Hypoglycemic coma E05.91 Hyperthyroidism with thyrotoxic crisis E16.2 Hypoglycemia E06.1 Subacute thyroiditis E87.0 Nonketotic hyperosmolar syndrome E06.3 Autoimmune thyroid disorder E87.2 Alcohol ketoacidosis E06.3 Hashimoto’s thyroiditis Diabetes Mellitus E06.3 Hashimoto’s struma E10.10 Diabetes type 1 with ketoacidosis E06.5 Chronic
    [Show full text]
  • Society for Endocrinology National Clinical Cases 2021
    Endocrine Abstracts June 2021 Volume 74 ISSN 1479-6848 (online) Society for Endocrinology National Clinical Cases 2021 22 June 2021, Online published by Online version available at bioscientifica www.endocrine-abstracts.org Volume 74 Endocrine Abstracts June 2021 Society for Endocrinology National Clinical Cases 2021 Tuesday 22 June 2021 Online Meeting Chairs Dr Anna Crown (Brighton) Dr Miles Levy (Leicester) Dr Annice Mukherjee (Manchester) Dr Michael O’Reilly (Dublin) Abstract Marking Panel Dr Kristien Boelart (Birmingham) Dr Karin Bradley (Bristol) Dr Simon Howell (Preston) Dr Andrew Lansdown (Cardiff) Dr Miles Levy (Leicester) Dr Daniel Morganstein (London) Dr Michael O’Reilly (Dublin) Professor Robert Semple (Edinburgh) Dr Peter Taylor (Cardiff) Dr Helen Turner (Oxford) Professor Bijay Vaidya (Exeter) Dr Nicola Zammitt (Edinburgh) Society for Endocrinology National Clinical Cases 2021 CONTENTS Society for Endocrinology National Clinical Cases 2021 Oral Communications ................................................. OC1–OC10 Highlighted Cases ................................................. NCC1–NCC71 AUTHOR INDEX Endocrine Abstracts (2021) Vol 74 Society for Endocrinology National Clinical Cases 2021 Oral Communications Endocrine Abstracts (2021) Vol 74 Society for Endocrinology National Clinical Cases 2021 OC1 lupus-anticoagulant. 5 days post-admission, in view of sudden onset lower A rare heterozygous IGFI variant causing postnatal growth failure and backache & worsening infection markers, repeat CT CAP was done which offering novel insights into IGF-I physiology revealed new bilateral adrenal haemorrhages. MRI adrenals revealed B/l adrenal 1 1 2 1 haemorrhages with fat stranding ,no underlying adrenal mass noted. Her 9am Emily Cottrell , Sumana Chatterjee , Vivian Hwa & Helen L. Storr ! 1 cortisol was 25, therefore she was started on IV hydrocortisone for acute Centre for Endocrinology, William Harvey Research Institute, Barts and adrenal insufficiency.
    [Show full text]
  • An Unusual Presentation of Thyroglossal Cyst -A Case Report
    Case Report An unusual presentation of thyroglossal cyst -A case report Shilpi Agrawal1, Haritosh K. Velankar2,*, Cassandra A. Carvalho3, Yessu Krishna Shetty4, Yogesh G. Dabholkar5 1Junior Resident, 2Ex HOD and present Head of Unit, 3Senior Resident, 4Lecturer, 5HOD, 1-4D.Y. Patil Medical Collage, Nerul, Navi Mumbai, Maharashtra, India *Correspondent Author: Email: [email protected] Abstract Introduction: Although thyroglossal cysts are very common in children and young adults, their presentation in the elderly is very rare and often goes undiagnosed. This may lead to incomplete excision and recurrence of the cyst, thereby increasing the risk for a malignancy. Here we present a case in an elderly patient, who presented to us with a midline neck swelling, whereas the histopathology report confirmed a thyroglossal cyst. Keywords: Thyroglossal cyst, Elderly, Midline neck swelling, Malignancy, Incomplete. Introduction Thyroglossal cyst is a fibrous cyst that forms from a persistent thyroglossal duct. Thyroglossal cysts can be defined as an irregular neck mass or a lump which develops from cells and tissues that are left over after the formation of the thyroid gland during developmental stages. Case Report A 66 years old male patient presented to our hospital, with complaints of midline neck swelling since 1 year. The swelling was insidious in onset and Fig. 2: Surface anatomy of the excised mass gradually progressive in nature. There was no history of difficulty in breathing, change in voice, thyroid disorder or associated medical pathology. On examination, the swelling had a smooth surface, 4x4 cm in size, extending from lower border of thyroid cartilage to 1.5 cm above the jugular notch, with no skin changes, no scars or sinuses, moves with deglutition.
    [Show full text]
  • Large Thyroglossal Duct Cyst: a Case Report Available Online: 2020.04.02 Published: 2020.05.02
    e-ISSN 1941-5923 © Am J Case Rep, 2020; 21: e919745 DOI: 10.12659/AJCR.919745 Received: 2019.08.29 Accepted: 2020.02.19 Large Thyroglossal Duct Cyst: A Case Report Available online: 2020.04.02 Published: 2020.05.02 Authors’ Contribution: ACDEF 1 Sarah Mortaja 1 College of Medicine, Alfaisal University, Riyadh, Saudi Arabia Study Design A ABCE 2 Haneen Sebeih 2 Department of Otolaryngology, Head and Neck Surgery, Ohud Hospital, Madinah, Data Collection B Saudi Arabia Statistical Analysis C ABEF 3 Nasser W. Alobida 3 Department of Otolaryngology, Head and Neck Surgery, King Fahad Medical City, Data Interpretation D ACDE 4 Khalid Al-Qahtani Riyadh, Saudi Arabia Manuscript Preparation E 4 Department of Otolaryngology Head and Neck Surgery, College of Medicine, Literature Search F King Saud University, Riyadh, Saudi Arabia Funds Collection G Corresponding Author: Sarah Mortaja, e-mail: [email protected] Conflict of interest: None declared Patient: Female, 36-year-old Final Diagnosis: Thyroglossal duct cyst Symptoms: Dysphagia • neck mass Medication: — Clinical Procedure: Sistrunk’s procedure Specialty: Otolaryngology Objective: Unusual clinical course Background: Thyroglossal duct cysts are the most common congenital neck cysts. They typically present in childhood and early adulthood, and average a size of 2–4 cm, but can also present in later adult life. Case Report: We present a case of a 36-year-old female patient with a very large midline neck mass, reaching the mandible superiorly. Patient history and physical examination, as well as computed tomography scan of her neck, con- firmed the diagnosis of large thyroglossal duct cyst. She underwent Sistrunk procedure for thyroglossal duct cyst excision, and the specimen was sent for histopathological evaluation, which confirmed the diagnosis.
    [Show full text]
  • Minor Surgical Conditions of Childhood Ajw Millar Ra Brown
    OPEN ACCESS TEXTBOOK OF GENERAL SURGERY MINOR SURGICAL CONDITIONS OF CHILDHOOD AJW MILLAR RA BROWN STERNOMASTOID `TUMOUR' Management (FIBRO- MATOSIS COLLI) AND A combination of active and postural TORTICOLLIS physiotherapy is successful in the vast majority of cases. Active: the child's Clinical evidence head is taken gently through a full This may present in three different range of movement (chin to shoulder, ways depending upon the age of the ear to shoulder on each side and patient. extension/flexion.) Postural: · In the neonate 2 - 3 weeks old a positioning such that the child is firm swelling is noticed in the neck encouraged to turn the head towards which is localized to the the affected side e.g. cot position, car sternomastoid muscle. Usually seat, etc. Facial asymmetry cannot be detected because of torticollis - expected to correct itself after the age `wry neck'. Occasionally presents of 5 years. In those cases which with facial and cranial asymmetry. present late or where no progress is · In the older infant there may be no obtained, the muscle is surgically history of a swelling but the divided. In the older child the sternomastoid muscle is now firm investing deep cervical fascia on that and foreshortened. `Wry neck' side is also divided. Less than 5% of · The older child may present with all cases diagnosed in infancy require torticollis. The face is rotated away surgery. It is important to continue from the affected side and the with physiotherapy after surgery. head tilted towards the affected side. This is due to the shortening THYROGLOSSAL CYST AND and fibrosis in the muscle with FISTULA facial and cranial asymmetry are usually apparent.
    [Show full text]
  • Historical Control Data on Non-Neoplastic Findings in Wistar Rats (Planned Sacrifices After 26 Weeks, Recovery)
    HISTORICAL CONTROL DATA ON NON-NEOPLASTIC FINDINGS IN WISTAR RATS (PLANNED SACRIFICES AFTER 26 WEEKS, RECOVERY) COMPILED FROM BIOASSAYS PERFORMED AT RCC LTD. ITINGEN/SWITZERLAND Historical Control Data on Non-Neoplastic Findings in Wistar Rats from 26-weeks Studies, Recovery Contents Table 1: Study Identification ........................................................................................................................................................................................................................................... 5 Table 2: Mortality Data ................................................................................................................................................................................................................................................... 6 Table 3: Type and Number of the Non-Neoplastic Lesions of the Brain........................................................................................................................................................................ 7 Table 4: Type and Number of the Non-Neoplastic Lesions of the Cerebellum. ............................................................................................................................................................. 8 Table 5: Type and Number of the Non-Neoplastic Lesions of the Cerebrum ................................................................................................................................................................ 9 Table 6: Type and Number of the
    [Show full text]
  • Congenital Cervical Cysts, Sinuses and Fistulae Stephanie P
    Otolaryngol Clin N Am 40 (2007) 161–176 Congenital Cervical Cysts, Sinuses and Fistulae Stephanie P. Acierno, MD, MPH, John H.T. Waldhausen, MD* Department of Surgery, Children’s Hospital and Regional Medical Center, University of Washington School of Medicine, G0035, 4800 Sand Point Way, NE, Seattle, WA 98105, USA Congenital cervical cysts, sinuses, and fistulae must be considered in the diagnosis of head and neck masses in children and adults. These include, in descending order of frequency, thyroglossal duct cysts, branchial cleft anomalies, dermoid cysts, and median cervical clefts. A thorough understand- ing of the embryology and anatomy of each of these lesions is necessary to provide accurate preoperative diagnosis and appropriate surgical therapy, which are essential to prevent recurrence. The following sections review each lesion, its embryology, anatomy, common presentation, evaluation, and the key points in surgical management. Thyroglossal duct anomalies Thyroglossal duct anomalies are the second most common pediatric neck mass, behind adenopathy in frequency [1]. Thyroglossal duct remnants occur in approximately 7% of the population, although only a minority of these is ever symptomatic [1]. Embryology The thyroid gland forms from a diverticulum (median thyroid anlage) lo- cated between the anterior and posterior muscle complexes of the tongue at week 3 of gestation. As the embryo grows, the diverticulum is displaced cau- dally into the neck and fuses with components from the fourth and fifth * Corresponding author. E-mail address: [email protected] (J.H.T. Waldhausen). 0030-6665/07/$ - see front matter Ó 2007 Elsevier Inc. All rights reserved. doi:10.1016/j.otc.2006.10.009 oto.theclinics.com 162 ACIERNO & WALDHAUSEN branchial pouches (lateral thyroid anlagen).
    [Show full text]
  • Thyroglossal Duct Cyst Revisited: a 13-Year Clinical Audit and Review Of
    id Diso ro rd y er h s T & f o T l h a e r n a r p u Journal of Thyroid Disorders & Therapy y o Mohamad et al., Thyroid Disorders Ther 2014, 3:1 J ISSN: 2167-7948 DOI: 10.4172/2167-7948.1000e114 Editorial Open Access Thyroglossal Duct Cyst Revisited: A 13-Year Clinical Audit and Review of Literature Irfan Mohamad1*, Aliyu Ango Yaroko1, Wan Faiziah Wan Abdul Rahman2, Nik Fariza Husna Nik Hassan1,4 and Ikhwan Sani Mohamad3 1Department of Otorhinolaryngology-Head & Neck Surgery, Universiti Sains Malaysia 2Department of Pathology, Universiti Sains Malaysia 3Department of Surgery, School of Medical Sciences, Universiti Sains Malaysia 4Speech Pathology Programme, School of Health Sciences, Universiti Sains Malaysia *Corresponding author: Dr. Irfan Mohamad, Department of Otorhinolaryngology-Head & Neck Surgery, School of Medical Sciences, Universiti Sains Malaysia Health Campus, 16150 Kota Bharu, Kelantan, Malaysia, Tel : 609-7676420; Fax: 609-7676424; E-mail: [email protected] Rec date: Feb 25, 2014, Acc date: Feb 25, 2014, Pub date: Feb 27, 2014 Copyright: © Mohamad I, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Introduction in all our patients. No surgical complications or recurrence was recorded in this series. Thyroglossal duct cysts (TDCs) are the most common congenital anomaly of the neck in childhood, representing more than 70% of congenital neck anomaly [1]. The cyst usually is a painless midline mass close to hyoid bone and slightly mobile.
    [Show full text]
  • Congenital Anomalies
    Congenital Anomalies 740 Anencephalus and similar anomalies 7400 Anencephalus and similar anomalies 74000 Absence of brain 74001 Acrania 74002 Anencephaly 74003 Hemlanencephaly 74008 Anencephalus - Other 7401 Craniorachischisis 7402 Iniencephaly 74020 Closed Iniencephaly 74021 Open Iniencephaly 74029 Iniencephaly - Unspecified 741 Spina bifida 7410 Spina bifida - With hydrocephalus 74100 Spina bifia aperta, any site, with hydrocephalus 74101 Spina bifida (cystica), any site, with Arnold Chiari malformation and hydrocephalus (Arnold Chiari malformation NOS) 74102 Spina bifida (cystica), any site, with stenosed aqueduct of Sylvius 74103 Spina bifida cystica, cervical, with unspecified hydrocephalus 74104 Spina bifida cystica, thoracic, with unspecified hydrocephalus 74105 Spina bifida - lumbar, with unspecified hydrocephalus 74106 Spina bifida cystica, sacral, with unspecified hydrocephalus 74107 Spina bifida of any site with hydrocephalus of late onset 74108 Spina bifida - With hydrocephalus - Other 74109 Spina bifida - With hydrocephalus - Unspecified 7419 Spina bifida - Without mention of hydrocephalus 74190 Spina bifida aperta - Without mention of hydrocephalus 74191 Spina bifida cystica, cervical - Without mention of hydrocephalus 74192 Spina bifida cystica, thoracic - Without mention of hydrocephalus 74193 Spina bifida cystica, lumbar - Without mention of hydrocephalus 74194 Spina bifida cystica, sacral - Without mention of hydrocephalus 74198 Spina bifida - Without mention of hydrocephalus - Other 74199 Spina bifida - Without mention
    [Show full text]