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Chronic lymphocytic leukemia, a rare cause of spontaneous rupture of the spleen.
Ayoub, Madani; Mabrouk, Mohamed Yassine; Abdelouahab, Hajar; Kamaoui, Imane; Achraf, Miry; Hamaz, Siham; Serraj, Khalid; Rachid, Jabi; Mohamed, Bouziane.
Afiliação
  • Ayoub M; Department of General Surgery, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Laboratory of Anatomy, Microsurgery and Surgery, Experimental and Medical Simulation (LAMCESM), Mohammed Ist University, Oujda, Morocco. Electronic address: madaniayoob23@gmail.com.
  • Mabrouk MY; Department of General Surgery, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Laboratory of Anatomy, Microsurgery and Surgery, Experimental and Medical Simulation (LAMCESM), Mohammed Ist University, Oujda, Morocco.
  • Abdelouahab H; Department of Radiology, Mohammed VI University Hospital, Oujda, Morocco.
  • Kamaoui I; Department of Radiology, Mohammed VI University Hospital, Oujda, Morocco.
  • Achraf M; Department of Anatomopathology, Mohammed VI University Hospital, Oujda, Morocco.
  • Hamaz S; Infectious Diseases, Immunohematology and Cellular Therapy Laboratory, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University of Oujda, Morocco.
  • Serraj K; Internal Medicine, Immunohematology and Cellular Therapy Laboratory, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University of Oujda, Morocco.
  • Rachid J; Department of General Surgery, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Laboratory of Anatomy, Microsurgery and Surgery, Experimental and Medical Simulation (LAMCESM), Mohammed Ist University, Oujda, Morocco.
  • Mohamed B; Department of General Surgery, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Laboratory of Anatomy, Microsurgery and Surgery, Experimental and Medical Simulation (LAMCESM), Mohammed Ist University, Oujda, Morocco.
Int J Surg Case Rep ; 96: 107315, 2022 Jul.
Article em En | MEDLINE | ID: mdl-35763971
ABSTRACT

INTRODUCTION:

Spleen Spontaneous Rupture SRS is a rare phenomenon in which the spleen ruptures without associated trauma. This pathology is rarely caused by Chronic Lymphocytic Leukemia. PRESENTATION OF THE CASE We present a case of a 59-year-old male patient with chronic Lymphocytic Leukemia, who was admitted with an acute abdomen whose clinical and paraclinical examinations revealed a spleen spontaneous rupture. The treatment consisted of a splenectomy.

DISCUSSION:

Spontaneous spleen rupture was first described by Rokitansky in 1861 and mentioned in many cases since, the common causes of non-traumatic Splenic rupture include myeloproliferative diseases, vasculitis, and infections. However, Chronic Lymphocytic Leukemia (CLL) remains an obscure cause of splenic rupture that requires unique attention. The diagnosis of splenic rupture should be considered in all patients with hematologic malignancies presenting with abrupt onset of abdominal pain, hemodynamic instability, or acute anemia. The choice between conservative treatment and splenectomy depends on different variables the etiology of the SRS, the hemodynamic stability, the amount of packed red blood cells transfused. Thus, an interventional approach can be advocated for a spontaneous splenic rupture over nonoperative management. Splenic embolization can provide patients with the advantages of both operative splenectomy and conservative management. The mortality rate from SRS is 12.2 %. Neoplastic pathologies were most significantly associated with fatal outcomes.

CONCLUSION:

The high mortality rate seems to be mainly related to the delayed diagnosis and/or the severity of the underlying pathology. Given its seriousness, it requires a rapid diagnosis and adapted management.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Int J Surg Case Rep Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Int J Surg Case Rep Ano de publicação: 2022 Tipo de documento: Article