Elizabeth G.K. Floodeen , Marshall F. Newman , Rafik Abdelsayed , Pratikkumar Patel
{"title":"Numb chin syndrome as initial symptom of T-cell acute lymphoblastic leukemia in a 14-year-old female: A case report","authors":"Elizabeth G.K. Floodeen , Marshall F. Newman , Rafik Abdelsayed , Pratikkumar Patel","doi":"10.1016/j.omsc.2022.100277","DOIUrl":null,"url":null,"abstract":"<div><p>Numb chin syndrome (NCS) has been described in the context of known malignancy or as a signal of disease recurrence; however, it is unusual to be the initial presenting symptom of malignancy. We offer a case report of an otherwise healthy 14-year old female who presented with NCS of seven months duration. Radiographic imaging showed a ill-defined “moth eaten” appearance of the mandible and incisional biopsy showed diffuse lymphocyte infiltrates. Immunohistologic staining performed was consistent with T-cell acute lymphoblastic leukemia/lymphoma (T-ALL), which was later confirmed with bone marrow aspirate. While traditionally the diagnosis of lymphoma was reserved only for bulky lesions with minimal disease of the peripheral blood and bone marrow, current trends have shifted to group lymphoblastic leukemia and lymphoma as a single disease process spectrum. After a review of the literature, no reports were identified of NCS as the only presenting symptom of T-ALL in a previously healthy child. We therefore propose an algorithm to guide clinicians in an accurate and timely diagnosis of this common pediatric malignancy.</p></div>","PeriodicalId":38030,"journal":{"name":"Oral and Maxillofacial Surgery Cases","volume":"8 4","pages":"Article 100277"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214541922000360/pdfft?md5=d4c16603f186b45d46d1e0984cf393ef&pid=1-s2.0-S2214541922000360-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oral and Maxillofacial Surgery Cases","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214541922000360","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Dentistry","Score":null,"Total":0}
引用次数: 0
Abstract
Numb chin syndrome (NCS) has been described in the context of known malignancy or as a signal of disease recurrence; however, it is unusual to be the initial presenting symptom of malignancy. We offer a case report of an otherwise healthy 14-year old female who presented with NCS of seven months duration. Radiographic imaging showed a ill-defined “moth eaten” appearance of the mandible and incisional biopsy showed diffuse lymphocyte infiltrates. Immunohistologic staining performed was consistent with T-cell acute lymphoblastic leukemia/lymphoma (T-ALL), which was later confirmed with bone marrow aspirate. While traditionally the diagnosis of lymphoma was reserved only for bulky lesions with minimal disease of the peripheral blood and bone marrow, current trends have shifted to group lymphoblastic leukemia and lymphoma as a single disease process spectrum. After a review of the literature, no reports were identified of NCS as the only presenting symptom of T-ALL in a previously healthy child. We therefore propose an algorithm to guide clinicians in an accurate and timely diagnosis of this common pediatric malignancy.
期刊介绍:
Oral and Maxillofacial Surgery Cases is a surgical journal dedicated to publishing case reports and case series only which must be original, educational, rare conditions or findings, or clinically interesting to an international audience of surgeons and clinicians. Case series can be prospective or retrospective and examine the outcomes of management or mechanisms in more than one patient. Case reports may include new or modified methodology and treatment, uncommon findings, and mechanisms. All case reports and case series will be peer reviewed for acceptance for publication in the Journal.