Bone Scintigraphy in the Examining of Treatment-Naive Pediatric Patients With Langerhans Cell Histiocytosis

Author:

Krylov A. S.1,Ryzhkov A. D.1,Kaspshik S. M.1,Krylova M. A.2,Stanyakina E. E.1,Dolguyshin M. B.1

Affiliation:

1. Clinical and Experimental Radiology Research Institute, Interventional Radiology Laboratory, Federal State Budgetary Institution «N.N. Blokhin National Medical Research Center of Oncology» оf the Ministry of Health of the Russian Federation

2. Children’s City Polyclinic No. 11 of the Moscow City Health Department

Abstract

Introduction: Histiocytosis is a heterogeneous group of rare diseases of unknown etiology. LCH is characterized by an abnormal proliferation of histiocytes (activated dendric cells and macrophages). Langerhans cell histiocytosis (LCH) is the most common form of histiocytosis, it is a potentially fatal diseases. Early detection of LCH plays an important role in its prognosis and outcome. However, the role of advanced methods of nuclear medicine in diagnosis of LCH is still to be researched. We have long-term experience in observing pediatric patients with LCH. Taking into the account the difficulty of diagnostic task for bone scintigraphy in identifying lytic bone destruction, we stated the following objective of the study.Purpose: Retrospective and prospective analysis of bone scintigraphy examinations of treatment-naive pediatric patients with LCH and calculate the diagnostic efficacy of bone scintigraphy. Material and methods: We analyzed 60 examinations of treatment-naive pediatric patients with proven case of LCH (2014-2019). The scanning was performed using whole body mode, 3 hours after intravenous injection of bone-seeking radiopharmaceutical 99mTc-MDP on Symbia E, T2 (Siemens, Germany). The median age was 5.6 years.Results: During examination we visualized 88 lesions with pathological level of accumulation of radiopharmaceutical in 60 patients. 84 with high level of accumulation (>120 %); 3 with slightly increased level of accumulation (100–120 %) and 1 with lower than normal level of accumulation (<100 %). The median level of accumulation of radiopharmaceutical was 268 %. Max level of accumulation was 1422 % (patient with subtotal involvement of femoral bone). Min — 60 % (patient with lytic destruction in orbital bone). During X-Ray we found out 97 pathological focuses of bone lytic destruction. In 3 patients with polyostotic form we found extra focuses on scintigraphy, which were confirmed with following examination and X-Ray. 8 lesions were not found on scintigraphy in 8 patients.Сonclusions: We evaluated diagnostic accuracy of bone scintigraphy with 99mTc-MDP in treatment-naïve pediatric patients with proven case of LCH. Sensitivity, specificity, NPV and PPV — 91.6, 50.0, 11.1, 98.6 %, respectively.

Publisher

Non-profit partnership Society of Interventional Oncoradiologists

Reference22 articles.

1. Львов АН, Волощук ИН, Варшавский ВА и др. Синусный гистиоцитоз (болезнь Розаи–Дорфмана): клиническое наблюдение. Вестник дерматологии и венерологии. 2001;(5):115-20. [Lvov AN, Voloshchuk IN, Varshavsky VA, et al. Sinus histiocytosis (Rosai-Dorfman disease): a clinical observation. Vestn Dermatol Venerol. 2011;(5):115-120. (In Russ.)].

2. Леменева ЗЛ, Иванов ОЛ, Мельниченко ГА и др. Множественные эндокринные нарушения при гистиоцитозе Х (болезни Хенда–Шюллера–Крисчена). Проблемы эндокринологии. 1982;28(6):57-8. [Lemeneva ZL, Ivanov OL, Melnichenko GA, et al. Multiple endocrine disorders in histiocytosis X (Hend — Schüller — Christian disease). Problems of Endocrinology. 1982;28(6):57-8. (In Russ.)].

3. Валиев ТТ, Попа АВ. Проект. Клинические рекомендации по диагностике и лечению детей, больных лангергансоклеточным гистиоцитозом. Общероссийский союз общественных объединений Ассоциация онкологов России. 2014. [Valiev TT, Popa AV. Project. Clinical guidelines for the diagnosis and treatment of children with Langerhans cell histiocytosis. All-Russian Union of Public Associations Russian Association of Oncologists. 2014. (In Russ). http://oncology-association.ru/files/clinical-guidelines_kids/gistiocitoz.pdf].

4. Haupt R (Leader and Editor), Astigarraga I, Schaefer E, et al. Langerhans Cell Histiocytosis (LCH) — Children. Guidelines for diagnosis, clinical workup and treatment during childhood; Version 1.1, March 2011. Euro Histio Net Work Group for LCH Guidelines. https://www.eurohistio.net/e1623/e1554/e1856/index_eng.html.

5. McGinnis LM, Nybakken G, Ma L, Arber DA. Frequency of MAP2K1, TP53, and U2AF1 Mutations in BRAF-mutated Langerhans Cell Histiocytosis: Further Characterizing the Genomic Landscape of LCH. Am J Surg Pathol. 2018;42(7):885-90. DOI: 10.1097/PAS.0000000000001057.

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