Literature DB >> 644372

Recurrent hemolytic anemia secondary to acessory spleens.

J B Bart, M F Appel.   

Abstract

A patient with recurrent hereditary spherocytosis due to a hypertrophied accessory spleen is presented. In patients in whom splenectomy is performed for hematologic disease, accessory spleens must be sought and removed. Recurrence of the inital disease should prompt a search for accessory spleens.

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Year:  1978        PMID： 644372     DOI： 10.1097/00007611-197805000-00038

Source DB:  PubMed          Journal:  South Med J        ISSN： 0038-4348            Impact factor:   0.954


  4 in total

1.  Complementary use of computerized tomography and technetium scanning in the diagnosis of accessory spleen.

Authors:  S N Joshi; M K Wolverson; R B Cusworth; S G Nair; R P Perrillo
Journal:  Dig Dis Sci       Date:  1980-11       Impact factor: 3.199

2.  Hereditary spherocytosis. Recent experience and current concepts of pathophysiology.

Authors:  R D Croom; C W McMillan; E P Orringer; G F Sheldon
Journal:  Ann Surg       Date:  1986-01       Impact factor: 12.969

3.  Preoperative computed tomography and scintigraphy to facilitate the detection of accessory spleen in patients with hematologic disorders.

Authors:  N Koyanagi; T Kanematsu; K Sugimachi
Journal:  Jpn J Surg       Date:  1988-01

4.  An intrapancreatic accessory spleen presenting as a rapidly growing pancreatic mass after splenectomy in a patient with hereditary spherocytosis: a case report and literature review.

Authors:  Yukihiro Tatekawa
Journal:  J Surg Case Rep       Date:  2018-02-23
  4 in total

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