CASE REPORT
Synchronous neoplasms in a paediatric patient
More details
Hide details
1
Student Scientific Society of the Department of Paediatric Haematology, Oncology, and Transplantology, Medical University of Lublin, Poland
2
Department of Paediatric Haematology, Oncology, and Transplantology, Medical University of Lublin, Poland
Submission date: 2023-07-10
Final revision date: 2023-10-10
Acceptance date: 2023-10-25
Publication date: 2024-03-05
Corresponding author
Aleksandra Dembowska
Aleksandra Dembowska, Student Scientific Society of the Department of Paediatric Haematology, Oncology, and Transplantology, Medical University of Lublin, 6 Gębali St., 20-093 Lublin, Poland
Pediatr Pol 2024;99(1):66-70
KEYWORDS
TOPICS
ABSTRACT
Cancer is the second leading cause of death in the paediatric population after injuries. 3–10% of them are multiple primary malignant neoplasms, which are a huge problem both in diagnosis and treatment. We present a case of a boy, nearly 2 years old, with synchronous coexistence of T-cell acute lymphoblastic leukaemia and Langerhans cell histiocytosis. During the M AIEOP BFM ALL 2017 Protocol, the patient suffered an injury to the right elbow joint. Despite the limb being provided with a plaster cast and orthopaedic intervention, local improvement was not achieved. The obtained result of the histopathological examination revealed a disseminated aggressive form of histiocytosis affecting the skeletal system and lungs. In the presence of non-specific symptoms for the diagnosed cancer, one should be vigilant and suspect the coexistence of another proliferative process, which may cause no improvement despite proper therapeutic management.
REFERENCES (19)
1.
Kichler K, Hnatyszyn M. The family of a child with leukemia – the perspective of the mother. Psychoonkologia 2015; 19: 169-174.
2.
Stachowicz-Stencel T, Krawczyk M, Balcerska A. Wczesna diagnostyka choroby nowotworowej u dzieci. Forum Med Rodz 2010;4: 431-437.
3.
Kapała A, Mężyk E, Kowalczyk A, et al. Maska reumatologiczna chorób nowotworowych u dzieci – obserwacje własne. For Reumatol 2016; 2: 130-135.
4.
Góra D, Figura N, Gregor M, Olszar M. Epidemiology of selected diseases cancer in children and adolescents in the Silesian Voivodeship in 2010 – 2019. Borgis N Pediatr 2021; 2: 3-10.
5.
Kuncman Ł, Danielska J, Kuncman W, et al. Synchronous occurrence of four malignancies in a 55-year-old woman with uterine cervical cancer. Case report and review of literature. Ginekol Pol 2016; 87: 314-317.
6.
Bruzgielewicz A, Chęciński P, Dąbrowski B, et al. Mnogie pierwotne nowotwory złośliwe u jednego pacjenta - opis przypadku. Pol Prz Otorynolaryngol 2015; 3: 35-38.
7.
Karrman K, Johansson B. Pediatric T-cell acute lymphoblastic leukemia. Gen Chrom Cancer 2017; 56: 89-116.
8.
Burkhardt B. Paediatric lymphoblastic T-cell leukaemia and lymphoma: one or two diseases? Br J Haematol 2010; 149: 653-668.
9.
Allen CE, Merad M, McClain KL. Langerhans-cell histiocytosis. N Engl J Med 2018; 379: 856-868.
11.
Anastasilakis AD, Tsoli M, Kaltsas G, Makras P. Bone metabolism in Langerhans cell histiocytosis. Endocr Connect 2018; 7: R246-R253.
12.
Raciborska A, Bilska K, Węcławek-Tompol J, et al. Clinical characteristics and outcome of pediatric patients diagnosed with Langerhans cell histiocytosis in pediatric hematology and oncology centers in Poland. BMC Cancer 2020; 20: 874.
13.
Bagnasco F, Zimmermann SY, Egeler RM, et al. The international dataset on the association between Langerhans Cell Histiocytosis and other malignancies. Data Brief 2022; 45: 108604.
14.
Trebo MM, Attarbaschi A, Mann G, et al. Histiocytosis following T-acute lymphoblastic leukemia: a BFM study. Leuk Lymphoma 2005; 46: 1735-1741.
15.
Kato M, Seki M, Yoshida K, et al. Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia. Br J Haematol 2016; 175: 169-172.
16.
Yokokawa Y, Taki T, Chinen Y, et al. Unique clonal relationship between T-cell acute lymphoblastic leukemia and subsequent Langerhans cell histiocytosis with TCR rearrangement and NOTCH1 mutation. Gen Chrom Cancer 2015; 54: 409-417.
17.
Rodig SJ, Payne EG, Degar BA, et al. Aggressive Langerhans cell histiocytosis following T-ALL: clonally related neoplasms with persistent expression of constitutively active NOTCH1. Am J Hematol 2008; 83: 116-121.
18.
Yohe SL, Chenault CB, Torlakovic EE, Asplund SL, McKenna RW. Langerhans cell histiocytosis in acute leukemias of ambiguous or myeloid lineage in adult patients: support for a possible clonal relationship. Mod Pathol 2014; 27: 651-656.
19.
Wada H, Masuda K, Satoh R, et al. Adult T-cell progenitors retain myeloid potential. Nature 2008; 452: 768-772.