ICD-10-CM 2010 Index Addenda
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Who, How and What of Pathology of Soft Tissue Sarcoma
Editorial Page 1 of 11 Who, how and what of pathology of soft tissue sarcoma Salvatore Lorenzo Renne Anatomic Pathology Unit, Humanitas Research Hospital, Humanitas University, Rozzano, MI 20089, Italy Correspondence to: Salvatore Lorenzo Renne. Adjunct Teaching Professor, Anatomic Pathology Unit, Humanitas Research Hospital, Humanitas University, Via Manzoni 56, Rozzano, MI 20089, Italy. Email: [email protected]. Submitted Aug 06, 2018. Accepted for publication Aug 23, 2018. doi: 10.21037/cco.2018.10.09 View this article at: http://dx.doi.org/10.21037/cco.2018.10.09 Introduction to soft tissue sarcoma (STS) adipocytes (lipoma, spindle cells lipoma, hibernoma, well- pathology differentiated liposarcoma (LPS), myxoid LPS, etc.). One chapter is dedicated to specific entities “of uncertain STS is a generic term that refers to a heterogeneous group differentiation” that are well-characterized entities that do of rare neoplastic diseases. The aim of this review is to not readily resemble any normal mesenchymal cells (as the discuss the role of pathology in the multidisciplinary Ewing sarcoma or the synovial sarcoma—a clear misnomer). management of STS patients. This will be done: (I) The last chapter is dedicated to those sarcomas that do illustrating the framework for the current classification; (II) not follow in any of the previously listed diagnosis and are examining the characteristics that allows an expert diagnosis; therefore called “undifferentiated/unclassified sarcomas” (III) describing the role of the sarcoma pathologist -
Complete Case of a Rare but Benign Soft Tissue Tumor
Hindawi Case Reports in Orthopedics Volume 2019, Article ID 6840693, 5 pages https://doi.org/10.1155/2019/6840693 Case Report Hibernoma of the Upper Extremity: Complete Case of a Rare but Benign Soft Tissue Tumor Thomas Reichel ,1 Kilian Rueckl,1 Annabel Fenwick,1,2 Niklas Vogt,3 Maximilian Rudert,1 and Piet Plumhoff1 1Department of Orthopedic Surgery, Koenig-Ludwig-Haus, University of Wuerzburg, Brettreichstraße 11, 97074 Wuerzburg, Germany 2Department of Trauma Surgery, Klinikum Augsburg, 86156 Augsburg, Germany 3Department of Pathology, University of Wuerzburg, 97080 Wuerzburg, Germany Correspondence should be addressed to Thomas Reichel; [email protected] Received 26 February 2019; Accepted 14 April 2019; Published 21 May 2019 Academic Editor: Elke R. Ahlmann Copyright © 2019 Thomas Reichel et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Hibernoma is a rare benign lipomatous tumor showing differentiation of brown fatty tissue. To the author’s best knowledge, there is no known case of malignant transformation or metastasis. Due to their slow, noninfiltrating growth hibernomas are often an incidental finding in the third or fourth decade of life. The vast majority are located in the thigh, neck, and periscapular region. A diagnostic workup includes ultrasound and contrast-enhanced MRI. Differential diagnosis is benign lipoma, well- differentiated liposarcoma, and rhabdomyoma. An incisional biopsy followed by marginal resection of the tumor is the standard of care, and recurrence after complete resection is not reported. The current paper presents diagnostic and intraoperative findings of a hibernoma of the upper arm and reviews similar reports in the current literature. -
Malignant Hidradenoma: a Report of Two Cases and Review of the Literature
ANTICANCER RESEARCH 26: 2217-2220 (2006) Malignant Hidradenoma: A Report of Two Cases and Review of the Literature I.E. LIAPAKIS1, D.P. KORKOLIS2, A. KOUTSOUMBI3, A. FIDA3, G. KOKKALIS1 and P.P. VASSILOPOULOS2 1Department of Plastic and Reconstructive Surgery, 2First Department of Surgical Oncology and 3Department of Surgical Pathology, Hellenic Anticancer Institute, "Saint Savvas" Hospital, Athens, Greece Abstract. Introduction: Malignant tumors of the sweat glands difficult (1). Clear cell hidradenoma is an extremely rare are very rare. Clear cell hidradenoma is a lesion with tumor with less than 50 cases reported (2, 3). histopathological features resembling those of eccrine poroma The cases of two patients, suffering from aggressive and eccrine spiradenoma. The biological behavior of the tumor dermal lesions invading the abdominal wall and the axillary is aggressive, with local recurrences reported in more than 50% region, are described here. Surgical resection and of the surgically-treated cases. Materials and Methods: Two histopathological examination ascertained the presence of patients are presented, the first with tumor in the right axillary malignant clear cell hidradenoma. In addition to these region, the second with a recurrent tumor of the abdominal cases, a review of the literature is also presented. wall. The first patient underwent wide excision with clear margins and axillary lymph node dissection and the second Case Reports patient underwent wide excision of the primary lesion and bilateral inguinal node dissection due to palpable nodes. Patient 1. Patient 1 was a 68-year-old Caucasian male who had Results: The patients had uneventful postoperative courses. No undergone excision of a rapidly growing, ulcerous lesion of the additional treatment was administered. -
PROPOSED REGULATION of the STATE BOARD of HEALTH LCB File No. R057-16
PROPOSED REGULATION OF THE STATE BOARD OF HEALTH LCB File No. R057-16 Section 1. Chapter 457 of NAC is hereby amended by adding thereto the following provision: 1. The Division may impose an administrative penalty of $5,000 against any person or organization who is responsible for reporting information on cancer who violates the provisions of NRS 457. 230 and 457.250. 2. The Division shall give notice in the manner set forth in NAC 439.345 before imposing any administrative penalty 3. Any person or organization upon whom the Division imposes an administrative penalty pursuant to this section may appeal the action pursuant to the procedures set forth in NAC 439.300 to 439. 395, inclusive. Section 2. NAC 457.010 is here by amended to read as follows: As used in NAC 457.010 to 457.150, inclusive, unless the context otherwise requires: 1. “Cancer” has the meaning ascribed to it in NRS 457.020. 2. “Division” means the Division of Public and Behavioral Health of the Department of Health and Human Services. 3. “Health care facility” has the meaning ascribed to it in NRS 457.020. 4. “[Malignant neoplasm” means a virulent or potentially virulent tumor, regardless of the tissue of origin. [4] “Medical laboratory” has the meaning ascribed to it in NRS 652.060. 5. “Neoplasm” means a virulent or potentially virulent tumor, regardless of the tissue of origin. 6. “[Physician] Provider of health care” means a [physician] provider of health care licensed pursuant to chapter [630 or 633] 629.031 of NRS. 7. “Registry” means the office in which the Chief Medical Officer conducts the program for reporting information on cancer and maintains records containing that information. -
Clinical and Imaging Evaluation of Nipple Discharge
REVIEW ARTICLE Evaluation of Nipple Discharge Clinical and Imaging Evaluation of Nipple Discharge Yi-Hong Chou, Chui-Mei Tiu*, Chii-Ming Chen1 Nipple discharge, the spontaneous release of fluid from the nipple, is a common presenting finding that may be caused by an underlying intraductal or juxtaductal pathology, hormonal imbalance, or a physiologic event. Spontaneous nipple discharge must be regarded as abnormal, although the cause is usually benign in most cases. Clinical evaluation based on careful history taking and physical examination, and observation of the macroscopic appearance of the discharge can help to determine if the discharge is physiologic or pathologic. Pathologic discharge can frequently be uni-orificial, localized to a single duct and to a unilateral breast. Careful assessment of the discharge is mandatory, including testing for occult blood and cytologic study for malignant cells. If the discharge is physiologic, reassurance of its benign nature should be given. When a pathologic discharge is suspected, the main goal is to exclude the possibility of carcinoma, which accounts for only a small proportion of cases with nipple discharge. If the woman has unilateral nipple discharge, ultrasound and mammography are frequently the first investigative steps. Cytology of the discharge is routine. Ultrasound is particularly useful for localizing the dilated duct, the possible intraductal or juxtaductal pathology, and for guidance of aspiration, biopsy, or preoperative wire localization. Galactography and magnetic resonance imaging can be selectively used in patients with problematic ultrasound and mammography results. Whenever there is an imaging-detected nodule or focal pathology in the duct or breast stroma, needle aspiration cytology, core needle biopsy, or excisional biopsy should be performed for diagnosis. -
F-MARC Football Medicine Manual 2Nd Edition F-MARC Football Medicine Manual 2Nd Edition 2 Editors - Authors - Contributors | Football Medicine Manual
F-MARC Football Medicine Manual 2nd Edition F-MARC Football Medicine Manual 2nd Edition 2 Editors - Authors - Contributors | Football Medicine Manual Football Medicine Manual Editors DVORAK Jiri Prof. Dr F-MARC, Schulthess Clinic Zurich, Switzerland JUNGE Astrid Dr F-MARC, Schulthess Clinic Zurich, Switzerland GRIMM Katharina Dr FIFA Medical Offi ce Zurich, Switzerland Authors 2nd Edition 2009 ACKERMAN Kathryn E. Harvard Medical School Harvard, USA BABWAH Terence Dr Sports Medicine and Injury Rehabilitation Clinic Macoya, Trinidad BAHR Roald Prof. Dr Oslo Sports Trauma Research Center Oslo, Norway BANGSBO Jens Prof. Dr University of Copenhagen Copenhagen, Denmark BÄRTSCH Peter Prof. Dr University of Heidelberg Heidelberg, Germany BIZZINI Mario PT Schulthess Clinic Zurich, Switzerland CHOMIAK Jiri Dr Orthopaedic University Hospital Bulovka Prague, Czech Republic DVORAK Jiri Prof. Dr F-MARC, Schulthess Klinik Zurich, Switzerland EDWARDS Tony Dr Adidas Sports Medicine Auckland, New Zealand ENGEBRETSEN Lars Prof. Dr Oslo Sports Trauma Research Center Oslo, Norway FULLER Colin Prof. Dr University of Nottingham Nottingham, England GRIMM Katharina Dr FIFA Medical Offi ce Zurich, Switzerland JUNGE Astrid Dr F-MARC, Schulthess Clinic Zurich, Switzerland KHAN Karim Prof. Dr Editor in Chief British Journal of Sports Medicine Sydney, Australia Editors - Authors - Contributors | Football Medicine Manual 3 KOLBE John Prof. Dr University of Auckland Auckland, New Zealand LÜSCHER Thomas Prof. Dr University of Zurich Zurich, Switzerland MANDELBAUM Bert Dr Santa Monica Orthopaedic and Sports Medicine Group Santa Monica, USA MAUGHAN Ron Prof. Dr University of Loughborough Loughborough, Great Britain PETERSON Lars Prof. Dr Gothenburg Medical Center Gothenburg, Sweden REILLY Thomas Prof. Dr Liverpool John Moores University Liverpool, Great Britain SALTIN Bengt Prof. -
University of Dundee Hidradenoma Masquerading Digital
CORE Metadata, citation and similar papers at core.ac.uk Provided by University of Dundee Online Publications University of Dundee Hidradenoma masquerading digital ganglion cyst Makaram, Navnit; Chaudhry, Iskander H.; Srinivasan, Makaram S. Published in: Annals of Medicine and Surgery DOI: 10.1016/j.amsu.2016.07.017 Publication date: 2016 Document Version Publisher's PDF, also known as Version of record Link to publication in Discovery Research Portal Citation for published version (APA): Makaram, N., Chaudhry, I. H., & Srinivasan, M. S. (2016). Hidradenoma masquerading digital ganglion cyst: a rare phenomenon. Annals of Medicine and Surgery , 10, 22-26. DOI: 10.1016/j.amsu.2016.07.017 General rights Copyright and moral rights for the publications made accessible in Discovery Research Portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from Discovery Research Portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain. • You may freely distribute the URL identifying the publication in the public portal. Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Download date: 17. Feb. 2017 Annals of Medicine and Surgery 10 (2016) 22e26 Contents lists available at ScienceDirect Annals of Medicine and Surgery journal homepage: www.annalsjournal.com Case report Hidradenoma masquerading digital ganglion cyst: A rare phenomenon * Navnit Makaram a, , Iskander H. -
Life Expectancy and Incidence of Malignant Disease Iv
LIFE EXPECTANCY AND INCIDENCE OF MALIGNANT DISEASE IV. CARCINOMAOF THE GENITO-URINARYTRACT CLAUDE E. WELCH,' M.D., AND IRA T. NATHANSON,? MS., M.D. (Front the Collis P. Huntington Memorial Hospital of Harvard University, and the Pondville State Hospitul, Wre~ztham,Mass.) In previous communications the life expectancy of patients with cancer of the breast (I), oral cavity (2), and gastro-intestinal tract (3) has been discussed. In the present paper the life expectancy of patients with carci- noma of the genito-urinary tract will be considered. The discussion will include cancer of the vulva, vagina, cervix and fundus uteri, ovary, penis, testicle, prostate, bladder, and kidney. All cases of cancer of these organs admitted to the Collis P. Huntington Memorial and Pondville Hospitals in the years 1912-1933 have been reviewed personally. It must again be stressed that these hospitals are organized strictly for the care of cancer patients. All those with cancer that apply are admitted for treatment; many of them have only terminal care. Only those cases in which a definite history of the date of onset could not be determined or in which the diagnosis was uncertain have been omitted in the present study. In compiling statistics on age and sex incidence all cases entering the hospitals before Jan. 1, 1936, have been included. The method of calculation of the life expectancy curves was fully described in the first paper (1). No at- tempt to evaluate the number of five-year survivals has been made, since many of the patients did not receive their initial treatment in these hospitals. -
Human Anatomy As Related to Tumor Formation Book Four
SEER Program Self Instructional Manual for Cancer Registrars Human Anatomy as Related to Tumor Formation Book Four Second Edition U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service National Institutesof Health SEER PROGRAM SELF-INSTRUCTIONAL MANUAL FOR CANCER REGISTRARS Book 4 - Human Anatomy as Related to Tumor Formation Second Edition Prepared by: SEER Program Cancer Statistics Branch National Cancer Institute Editor in Chief: Evelyn M. Shambaugh, M.A., CTR Cancer Statistics Branch National Cancer Institute Assisted by Self-Instructional Manual Committee: Dr. Robert F. Ryan, Emeritus Professor of Surgery Tulane University School of Medicine New Orleans, Louisiana Mildred A. Weiss Los Angeles, California Mary A. Kruse Bethesda, Maryland Jean Cicero, ART, CTR Health Data Systems Professional Services Riverdale, Maryland Pat Kenny Medical Illustrator for Division of Research Services National Institutes of Health CONTENTS BOOK 4: HUMAN ANATOMY AS RELATED TO TUMOR FORMATION Page Section A--Objectives and Content of Book 4 ............................... 1 Section B--Terms Used to Indicate Body Location and Position .................. 5 Section C--The Integumentary System ..................................... 19 Section D--The Lymphatic System ....................................... 51 Section E--The Cardiovascular System ..................................... 97 Section F--The Respiratory System ....................................... 129 Section G--The Digestive System ......................................... 163 Section -
Eyelid Conjunctival Tumors
EYELID &CONJUNCTIVAL TUMORS PHOTOGRAPHIC ATLAS Dr. Olivier Galatoire Dr. Christine Levy-Gabriel Dr. Mathieu Zmuda EYELID & CONJUNCTIVAL TUMORS 4 EYELID & CONJUNCTIVAL TUMORS Dear readers, All rights of translation, adaptation, or reproduction by any means are reserved in all countries. The reproduction or representation, in whole or in part and by any means, of any of the pages published in the present book without the prior written consent of the publisher, is prohibited and illegal and would constitute an infringement. Only reproductions strictly reserved for the private use of the copier and not intended for collective use, and short analyses and quotations justified by the illustrative or scientific nature of the work in which they are incorporated, are authorized (Law of March 11, 1957 art. 40 and 41 and Criminal Code art. 425). EYELID & CONJUNCTIVAL TUMORS EYELID & CONJUNCTIVAL TUMORS 5 6 EYELID & CONJUNCTIVAL TUMORS Foreword Dr. Serge Morax I am honored to introduce this Photographic Atlas of palpebral and conjunctival tumors,which is the culmination of the close collaboration between Drs. Olivier Galatoire and Mathieu Zmuda of the A. de Rothschild Ophthalmological Foundation and Dr. Christine Levy-Gabriel of the Curie Institute. The subject is now of unquestionable importance and evidently of great interest to Ophthalmologists, whether they are orbital- palpebral specialists or not. Indeed, errors or delays in the diagnosis of tumor pathologies are relatively common and the consequences can be serious in the case of malignant tumors, especially carcinomas. Swift diagnosis and anatomopathological confirmation will lead to a treatment, discussed in multidisciplinary team meetings, ranging from surgery to radiotherapy. -
Aderomyoma of the Common Bile Duct --Report of a Case
Yamanashl Med. J. 4 (2), 83"v87, 1989 Case Report AdeRomyoma of the Common Bile Duct --Report of a Case Yoshiro MATsuMoTe, Masatoshi MoGAKi, Hidehisa AoyAMA, Takayoshi SEKmAwA, Katsnhiko SuGAHARA, Koichi SuDAi), and Masayuki FuJiNo2) DePa,rt･ment of Surge7pu. i)DePartment of Pathology, 2)DePartment of lnte7"nal Medicine, YamanasJzi Medical Coglege, Tamaho, Nakakoma, Ya?nanashi 409-38, JaPan Abstract: Adenomyomas in the extrahepatic biie duc£ are extremely rare. In a 75-year- old male with acute cholangitis due to adenomyoma £erming a protruding lesion iR the terminal bile duct, pamacreatoduodenectomy was carried out, resulting complete cure, Key words: Adenomyoma of the common bile duct, Early bile dact cancer, Obstructive jaundice formed, aRd £rom the histologic examina- INTRODUCTION tion of the surgical specimen, adenomyoma Adenomyoma in the biliary ductal system of the common bile duct was confirmed. is most freguently fouRd in the gallbladder. Although beRign neoplasma o£ the bile The gallbiadder wall is more abuRdant in duct system are uncommon, the tumors are muscle fibers than is the wall o£ the bile clinically very important because they can duct. Adenomyoma in the gallbladder is cause obstructive jaundice4) and require knowlt to be closely re}ated to the forma- differentiation £rom eary cancer of the bile tion of gallstones. In other parts of the duct. biliary ductal system, kex4xeve]-, adeno- We report here the surgical results and myoma is very rarei)･2), although a few pathologic findings in a case of adeno- cases of a tumor arising from the papil}a myoma of the terminal bile duct. of Vater3) have beelt reported. -
TUMOR and STAGING DATA Primary Site Code
SECTION IV - TUMOR and STAGING DATA Primary Site Code NAACCR Version 11.1 field "Primary Site", Item 400, columns 291-294 It is unclear how the 2007 MP/H rules may alter rules for assigning the best Primary Site Formatted: Left Code to each primary. Continue to use the following rules until new rules are issued. Enter the code for the site of origin from the Topography section of ICD-O-3. [Note that ICD-O-2 code C14.1, laryngopharynx, should not be used for diagnoses made on or after January 1, 1995. "Laryngopharynx" became an equivalent term under C13.9 (hypopharynx, NOS) as of this diagnosis date. Code C14.1 is not an ICD-O-3 code.] Enter the site code that matches the narrative primary site indicated in the medical record, or the site code most appropriate for the case. Site codes are found in ICD-O-3's Numerical Lists - Topography section (pages 45-65) and in its Alphabetic Index (pages 105-218). In ICD-O-3 primary site codes consist of the letter "C" followed by two digits, a decimal point, and a third digit. "C" should be entered but the decimal point should not be entered. Example: The primary site is "cardia of stomach". Look this up in the Alphabetic Index of ICD-O-3 under "stomach" or "cardia", and the corresponding code "C16.0" is found. Enter C160. Most sites include a third digit of "8" to be used for single tumors that overlap the boundaries of two or more anatomically contiguous subsites and whose exact point of origin cannot be determined, unless the combination of sites is specifically indexed elsewhere.