SciELO - Scientific Electronic Library Online

 
vol.104 issue8Endoscopic removal of intrauterine device penetrated through the rectal wallGiant duodenal ulcer perforation: a case of innovative repair with an antrum gastric patch author indexsubject indexarticles search
Home Pagealphabetic serial listing  

My SciELO

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Revista Española de Enfermedades Digestivas

Print version ISSN 1130-0108

Rev. esp. enferm. dig. vol.104 n.8 Madrid Aug. 2012

http://dx.doi.org/10.4321/S1130-01082012000800008 

PICTURES IN DIGESTIVE PATHOLOGY

 

Giant splenomegaly and non-Hodking's lymphoma

Esplenomegalia gigante y linfoma no Hodgkin

 

 

Luis Erik Álvarez-Burneo, Luis Kerlin Mercedes and Armando Arce-Álvarez

Department of General Surgery. Hospital Virgen de la Luz. Cuenca, Spain

 

 

Case report

A 35-year-old male presented to our clinic with asthenia, hyporexia, and weight loss (3 kg in two months) of one month duration. Physical examination was positive for an abdominal mass that occupied left side of abdomen, right iliac fossa and flank consistent with splenomegaly. Blood tests showed moderated anemia (Hb: 10 g/dL) and hypercalcemia (Ca: 13.1 mg/dL). Chest/abdominal CT scan revealed splenomegaly of 27 cm major axis with multiple hypodense areas and hiliar splenic adenopathies about 17-28 cm size (Fig. 1). Presumptive diagnosis of lymphoma was established and diagnostic/therapeutic splenectomy was scheduled.

 

 

Splenic resection was performed without complication via a subcostal laparotomy using an "in situ" technique (Fig. 2). Pathology returned as a diffuse large B-cell lymphoma and the patient was started on combined chemotherapy treatment (CHOP and rituximab).

 

 

Discussion

Diffuse large B-cell lymphoma is the most frequent variety of non-Hodgkin's lymphoma, representing approximately 33% of all cases (1). Presumptive diagnosis of lymphoma is based on clinical presentation, blood tests, and imaging. Splenectomy is necessary for a definitive anatomopathological diagnosis (1,2) in addition to being therapeutic (solves problems related with splenomegaly and hypersplenism) (3,4). After splenectomy blood counts return to normal values, transfusional requirements are reduced, and subsequent chemotherapy tolerance is improved (1,3,4).

Surgical approach using "in situ" technique is recommended for this kind of surgery (giant spleen and programmed surgery) (5).

 

References

1. Le Gouill S. Mantle cell lymphoma: an overview from diagnosis to future therapies. La Revue de Médecine Interne 2010;31:615-20.         [ Links ]

2. Iriyama N, Horikoshi A, Hatta Y, Kobayashi Y, Sawada S, Takeuchi J. Localized, splenic, diffuse large B-cell lymphoma presenting with hypersplenism: risk and benefit of splenectomy. Internal Medicine 2010;49:1027-30.         [ Links ]

3. Pottakkat B, Kashyap R, Kumar A, Sikora S , Saxena R, Kapoor V. Redefining the role of splenectomy in patients with idiopathic splenomegaly. ANZ Journal of Surgery 2006;76:679-82.         [ Links ]

4. Carr JA, Shuarafa M, Velanovich V. Surgical indications in idiopathic splenomegaly. Archives of Surgery 2002;137:64-8.         [ Links ]

5. Breil P. Splénectomie. Techniques chirurgicales- Appareil Digestif. Encycl Méd Chir. Paris-France: Elsevier; 1997.p. 40-750, 10 p.         [ Links ]

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License