Cargando…

Partial Splenectomy in the treatment of an adult with β thalassemia intermedia: A case report

INTRODUCTION: Thalassemia is a common disease which treatment is often based on splenectomy. The risks associated with total splenectomy stimulated partial splenectomy as a potentially alternative therapy. CASE PRESENTATION: A 45 year-old female patient with long term follow-up for β thalassemia int...

Descripción completa

Detalles Bibliográficos
Autores principales:	Correia, João Guardado, Moreira, Nídia, Costa Almeida, Carlos Eduardo, Reis, Luís Simões
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2017
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702856/ https://www.ncbi.nlm.nih.gov/pubmed/29546013 http://dx.doi.org/10.1016/j.ijscr.2017.11.011

Ejemplares similares

Thalassemia Intermedia: Chelator or Not?
por: Lee, Yen-Chien, et al.
Publicado: (2022)

Hypothyroidism in β-Thalassemia Intermedia Patients with and without Hydroxyurea
por: Zekavat, Omid Reza, et al.
Publicado: (2014)

β-Thalassemia Intermedia: A Bird’s-Eye View
por: Haddad, Anthony, et al.
Publicado: (2014)

Endocrine Function in Thalassemia Intermedia
por: Karamifar, H., et al.
Publicado: (2006)

β-Thalassemia Intermedia: Interaction of α-Globin Gene Triplication With β-thalassemia Heterozygous in Spain
por: Ropero, Paloma, et al.
Publicado: (2022)

Molecular characterization of β-thalassemia intermedia in the West Bank, Palestine
por: Faraon, Rashail, et al.
Publicado: (2019)

CMR survey in Thalassemia Intermedia patients
por: Meloni, Antonella, et al.
Publicado: (2014)

Laparoscopic splenectomy in patients of β thalassemia: Our experience
por: Patle, Nirmal M, et al.
Publicado: (2010)

Did the Proband Have Thalassemia Intermedia or Severe Thalassemia Trait?
por: Özsoylu, Şinasi
Publicado: (2012)

β-Thalassemia Intermedia in Northern Iraq: A Single Center Experience
por: Al-Allawi, Nasir A. S., et al.
Publicado: (2014)

Cyclic headaches in β-thalassemia intermedia case presenting as moyamoya syndrome
por: Akpınar, Süha, et al.
Publicado: (2015)

Endocrine and Bone Complications in β-Thalassemia Intermedia: Current Understanding and Treatment
por: Inati, Adlette, et al.
Publicado: (2015)

Three Mexican Families with β thalassemia intermedia with different molecular basis
por: de la Torre, Lourdes del Carmen Rizo, et al.
Publicado: (2020)

Renal Dysfunction in Pediatric Patients in Iraq With β-Thalassemia Major and Intermedia
por: Shaalan, Mohammad G, et al.
Publicado: (2022)

Stroke propensity in the Th3+/ mouse model of β-thalassemia intermedia
por: Sun, Yu-Yo, et al.
Publicado: (2022)

Rare Presentation of β-Thalassemia Intermedia With a Phenotype of Dilated Cardiomyopathy
por: Nakaya, Yuichiro, et al.
Publicado: (2023)

The Frequency of Adrenal Insufficiency in Adolescents and Young Adults with Thalassemia Major versus Thalassemia Intermedia in Iran
por: Matin, Sara, et al.
Publicado: (2015)

Evaluation of Cardiac Function in Patients with Thalassemia Intermedia
por: Nouri, NM, et al.
Publicado: (2013)

Secondary Haemochromatosis in a Patient with Thalassemia Intermedia
por: ROTARU, IONELA, et al.
Publicado: (2014)

Protein C and S levels in patients with Thalassemia intermedia
por: Mohammed, Nawsherwan Sadiq
Publicado: (2022)

Acute lymphoblastic leukemia in a β-thalassemia intermedia child: A case report
por: Sherief, Laila M, et al.
Publicado: (2020)

Early Predictors of Renal Dysfunction in Egyptian Patients with β-Thalassemia Major and Intermedia
por: Tantawy, Azza A.G., et al.
Publicado: (2014)

Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia
por: Hançer, Veysel Sabri, et al.
Publicado: (2020)

Acute Promyelocytic Leukemia in a Woman with Thalassemia Intermedia: Case Report and Review of Literature on Hematological Malignancies in β-Thalassemia Patients
por: Pellegrino, Claudio, et al.
Publicado: (2022)

The effect of splenectomy on complement regulatory proteins in erythrocytes in β-thalassemia major
por: Kurtoğllu, Ayşegül Uğur, et al.
Publicado: (2018)

Echocardiographic evaluation of thalassemia intermedia patients in Duhok, Iraq
por: Mohammad, Ameen Mosa
Publicado: (2014)

Tophaceous gout in thalassemia intermedia: a rare association
por: Mishra, Vikas, et al.
Publicado: (2016)

Gaucher-like Cells in Thalassemia Intermedia: Is It a Challenge?
por: Komninaka, Veroniki, et al.
Publicado: (2023)

PB2238: ΒETA-THALASSEMIA INTERMEDIA: INTERACTION OF ΑLPHA-GLOBIN GENE TRIPLICATION WITH ΒETA-THALASSEMIA HETEROZYGOUS IN SPAIN
por: Ropero, P., et al.
Publicado: (2022)

Therapeutic potential of silymarin as a natural iron‐chelating agent in β‐thalassemia intermedia
por: Reisi, Nahid, et al.
Publicado: (2022)

Side effects of hydroxyurea in patients with Thalassemia major and thalassemia intermedia and sickle cell anemia
por: Ghasemi, A, et al.
Publicado: (2014)

Beta-Thalassemia Intermedia: A Single Thalassemia Center Experience from Northeastern Iraq
por: Amin, Shaema Salih, et al.
Publicado: (2020)

Anaesthetic management of a patient with Eisenmenger syndrome and β-thalassemia major for splenectomy
por: Gupta, Nishkarsh, et al.
Publicado: (2011)

Frequency of Cholelithiasis in Patients With Beta-Thalassemia Intermedia With and Without Hydroxyurea
por: Khavari, Maryam, et al.
Publicado: (2014)

Dysregulation of the RANKL/RANK/OPG axis in thalassemia intermedia patients
por: Alfaqih, Mahmoud A., et al.
Publicado: (2018)

Subclinical Left Ventricular Dysfunction in Children and Adolescence With Thalassemia Intermedia
por: Isa Tafreshi, Roya, et al.
Publicado: (2022)

P1456: MULTIPARAMETRIC CMR AND CARDIAC COMPLICATIONS IN THALASSEMIA INTERMEDIA
por: Meloni, Antonella, et al.
Publicado: (2023)

Double heterozygocity for hemoglobin C and beta thalassemia dominant: A rare case of thalassemia intermedia
por: Agapidou, Alexandra, et al.
Publicado: (2018)

Corrigendum to “Beta-Thalassemia Intermedia: A Single Thalassemia Center Experience from Northeastern Iraq”
por: Amin, Shaema Salih, et al.
Publicado: (2020)

Long-Term Health-Related Quality of Life and Clinical Outcomes in Patients with β-Thalassemia after Splenectomy
por: Caocci, Giovanni, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_2mv0che39gl3f5jb6si46suthj