The Spectrum of Lung Involvement in Collagen Vascular-Like Diseases Following Allogeneic Hematopoietic Stem Cell Transplantation Report of 6 Cases and Review of the Literature

被引:12
作者
Bergeron, Anne [1 ]
Bengoufa, Djaouida [2 ]
Feuillet, Severine [1 ]
Meignin, Veronique [3 ]
de latour, Regis Peffault [4 ]
Rybojad, Michel [5 ]
Gossot, Dominique [7 ]
Azoulay, Elie [6 ]
Socie, Gerard [4 ]
Tazi, Abdellatif [1 ]
机构
[1] Univ Paris 07, Hop St Louis, AP HP, UFR Denis Diderot,Serv Pneumol, F-75475 Paris 10, France
[2] Univ Paris 07, Hop St Louis, AP HP, UFR Denis Diderot,Serv Immunol, F-75475 Paris 10, France
[3] Univ Paris 07, Hop St Louis, AP HP, UFR Denis Diderot,Serv Pathol, F-75475 Paris 10, France
[4] Univ Paris 07, Hop St Louis, AP HP, UFR Denis Diderot,Serv Hematol Greffe Moelle, F-75475 Paris 10, France
[5] Univ Paris 07, Hop St Louis, AP HP, UFR Denis Diderot,Serv Dermatol, F-75475 Paris 10, France
[6] Univ Paris 07, Hop St Louis, AP HP, UFR Denis Diderot,Serv Reanimat, F-75475 Paris 10, France
[7] Inst Mutualiste Montsouris, Serv Chirurg Thorac, Paris, France
关键词
VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; CONSENSUS DEVELOPMENT PROJECT; SJOGREN-LIKE SYNDROME; CHRONIC GRAFT; ACUTE POLYMYOSITIS; CLINICAL-TRIALS; MANIFESTATION; MYOSITIS; AUTOIMMUNITY;
D O I
10.1097/MD.0b013e31821160af
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multisystem autoimmune diseases occurring after allogeneic hematopoietic stem cell transplantation are infrequent, late-onset manifestations that resemble well-defined collagen vascular disorders. Because the lung is frequently involved in the course of connective tissue disorders, we focused on lung manifestations occurring in autoimmune diseases following allogeneic stem cell transplantation. In the present series, we report 6 patients with systemic lupus erythematous, mixed connective tissue disease, Sjogren syndrome, polymyositis, and ANCA-positive vasculitis who presented with a spectrum of pulmonary manifestations affecting the airways, lung parenchyma, and probably respiratory muscles. We identified 3 different histopathologic patterns of interstitial pneumonia consistent with the underlying autoimmune disorder: lymphocytic interstitial pneumonia and non-specific interstitial pneumonia in 2 patients with Sjogren syndrome and diffuse alveolar damage in 1 patient with ANCA-positive vasculitis. These lung manifestations had poor prognoses. Further studies are needed to determine the optimal therapy for these complications.
引用
收藏
页码:146 / 157
页数:12
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