Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or Consequence

Background: Graves’ disease (GD)-related bone marrow injury presents usually as agranulocytosis or less commonly as pancytopenia. However, acute lymphoblastic leukemia (ALL) has been reported recently in an adult patient with GD. The underlying pathogenesis is not fully understood. Nevertheless, the...

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Main Authors: Ghassan Faisal Fadlalbari, Samar Sabir Hassan, Asmahan T. Abdalla, Samar Omer Abusamra, Abeer Mohamed Abdalrhman, Mohamed Ahmed Abdullah
Format: Article
Language:English
Published: Karger Publishers 2023-01-01
Series:Dubai Diabetes and Endocrinology Journal
Subjects:
Online Access:https://www.karger.com/Article/FullText/527187
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author Ghassan Faisal Fadlalbari
Samar Sabir Hassan
Asmahan T. Abdalla
Samar Omer Abusamra
Abeer Mohamed Abdalrhman
Mohamed Ahmed Abdullah
author_facet Ghassan Faisal Fadlalbari
Samar Sabir Hassan
Asmahan T. Abdalla
Samar Omer Abusamra
Abeer Mohamed Abdalrhman
Mohamed Ahmed Abdullah
author_sort Ghassan Faisal Fadlalbari
collection DOAJ
description Background: Graves’ disease (GD)-related bone marrow injury presents usually as agranulocytosis or less commonly as pancytopenia. However, acute lymphoblastic leukemia (ALL) has been reported recently in an adult patient with GD. The underlying pathogenesis is not fully understood. Nevertheless, the harmful effects of anti-thyroid drugs or autoimmune reaction to bone marrow cells are anticipated to be the causative factors. Case Presentation: We report a 16.5-year-old girl with GD who was on carbimazole for the first 14 months of her illness, with irregular follow-up; then it was withdrawn because she developed hypothyroidism. Meanwhile, she developed severe anemia without fever which necessitated blood transfusion. Eight months later, she presented with thyrotoxicosis relapse, febrile illness, bone pain, and pancytopenia which was proved to be ALL on bone marrow examination. Conclusion: The presence of ALL in a young GD patient is an unprecedented event. Although it is difficult to demonstrate the causality between them, need for further studies cannot be denied.
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spelling doaj.art-adaf56516723406495b5eafca7421f372023-02-02T12:54:55ZengKarger PublishersDubai Diabetes and Endocrinology Journal2673-17972673-17382023-01-0128414314610.1159/000527187527187Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or ConsequenceGhassan Faisal Fadlalbari0https://orcid.org/0000-0003-0823-1682Samar Sabir Hassan1Asmahan T. Abdalla2https://orcid.org/0000-0001-5770-1340Samar Omer Abusamra3Abeer Mohamed Abdalrhman4Mohamed Ahmed Abdullah5https://orcid.org/0000-0001-7121-8216Department of Pediatric Endocrinology, Gaafar Ibnauf Pediatric Tertiary Hospital, Khartoum, SudanDepartment of Pediatric Endocrinology, Gaafar Ibnauf Pediatric Tertiary Hospital, Khartoum, SudanDepartment of Pediatric Endocrinology, Gaafar Ibnauf Pediatric Tertiary Hospital, Khartoum, SudanDepartment of Pediatric Endocrinology, Gaafar Ibnauf Pediatric Tertiary Hospital, Khartoum, SudanDepartment of Pediatric Endocrinology, Gaafar Ibnauf Pediatric Tertiary Hospital, Khartoum, SudanDepartment of Pediatric Endocrinology, Gaafar Ibnauf Pediatric Tertiary Hospital, Khartoum, SudanBackground: Graves’ disease (GD)-related bone marrow injury presents usually as agranulocytosis or less commonly as pancytopenia. However, acute lymphoblastic leukemia (ALL) has been reported recently in an adult patient with GD. The underlying pathogenesis is not fully understood. Nevertheless, the harmful effects of anti-thyroid drugs or autoimmune reaction to bone marrow cells are anticipated to be the causative factors. Case Presentation: We report a 16.5-year-old girl with GD who was on carbimazole for the first 14 months of her illness, with irregular follow-up; then it was withdrawn because she developed hypothyroidism. Meanwhile, she developed severe anemia without fever which necessitated blood transfusion. Eight months later, she presented with thyrotoxicosis relapse, febrile illness, bone pain, and pancytopenia which was proved to be ALL on bone marrow examination. Conclusion: The presence of ALL in a young GD patient is an unprecedented event. Although it is difficult to demonstrate the causality between them, need for further studies cannot be denied.https://www.karger.com/Article/FullText/527187graves’ diseaseacute lymphoblastic leukemiaadolescentrelapse
spellingShingle Ghassan Faisal Fadlalbari
Samar Sabir Hassan
Asmahan T. Abdalla
Samar Omer Abusamra
Abeer Mohamed Abdalrhman
Mohamed Ahmed Abdullah
Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or Consequence
Dubai Diabetes and Endocrinology Journal
graves’ disease
acute lymphoblastic leukemia
adolescent
relapse
title Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or Consequence
title_full Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or Consequence
title_fullStr Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or Consequence
title_full_unstemmed Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or Consequence
title_short Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or Consequence
title_sort acute lymphoblastic leukemia in an adolescent girl with graves disease a coincidence or consequence
topic graves’ disease
acute lymphoblastic leukemia
adolescent
relapse
url https://www.karger.com/Article/FullText/527187
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