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Surgical resection of extramedullary haematopoiesis in the posterior mediastinum
Author(s) -
Matsumoto Ryoichi,
Yoshiyama Koichi,
Yokoyama Shintaro,
Mitsuoka Masahiro,
Takamori Shinzo,
Akagi Yoshito
Publication year - 2018
Publication title -
respirology case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.304
H-Index - 9
ISSN - 2051-3380
DOI - 10.1002/rcr2.358
Subject(s) - medicine , hereditary spherocytosis , extramedullary hematopoiesis , mediastinum , haematopoiesis , mediastinal diseases , pathological , surgery , radiology , pathology , stem cell , biology , genetics
Extramedullary haematopoiesis is a rare disease that is usually associated with haematologic disorders such as thalassemia, myelodysplastic syndrome, and hereditary spherocytosis. It frequently occurs in the liver, spleen, and lymph nodes. Rarely, it occurs in the posterior mediastinum. We report the case of a 59‐year‐old man with lateral posterior mediastinal masses that were incidentally detected during treatment for hereditary spherocytosis. We performed video‐assisted thoracic surgery to confirm the diagnosis and differentiate the masses from neurogenic tumours and other posterior mediastinal diseases. The pathological findings were consistent with intrathoracic extramedullary haematopoiesis. Although extramedullary haematopoiesis can be managed without interventions, surgery may be required in some cases. In such cases, video‐assisted thoracoscopic surgery is advised because it is a useful and less invasive procedure.

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