Pathologic assessment of vasculopathies in pulmonary hypertension

被引:498
作者
Pietra, GG
Capron, F
Stewart, S
Leone, O
Humbert, M
Robbins, IM
Reid, LM
Tuder, RM
机构
[1] Univ Penn, Sch Med, Dept Pathol, Philadelphia, PA 19104 USA
[2] Hop Pitie, Serv Anat Pathol, F-75651 Paris 13, France
[3] Papworth Hosp, Cambridge CB3 8RE, England
[4] Azienda Osped S Orsola Malpighi Bologna, Dept Pathol, Bologna, Italy
[5] Univ Paris Sud, Hop Paris, Hop Antoine Beclere, Serv Pneumol & Reanimat Resp, Clamart, France
[6] Vanderbilt Univ, Med Ctr, Adult Pulm Hypertens Ctr, Nashville, TN USA
[7] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[8] Johns Hopkins Univ, Sch Med, Div Cardiopulm Pathol, Baltimore, MD USA
关键词
D O I
10.1016/j.jacc.2004.02.033
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pulmonary arterial hypertension (PAH) includes various forms of pulmonary hypertension of different etiology but similar clinical presentation and functional derangement. Histopathological vascular changes in all forms of PAH are qualitatively similar but with quantitative differences in the distribution and prevalence of pathological changes in various portions of the pulmonary vascular bed. The documentation of these topographic variations in the response of the pulmonary vasculature to injury may be important to understand the pathogenesis of the various subsets of PAR To standardize the precise histopathological documentation of the pulmonary vasculopathy in PAH we propose a histopathological classification that includes both the predominant segment of the pulmonary vasculature affected and the possible coexistence of pathological changes in other vascular segments. (C) 2004 by the American College of Cardiology Foundation.
引用
收藏
页码:25S / 32S
页数:8
相关论文
共 33 条
[11]  
FRI MG, 2002, CIRC RES, V90, P1189
[12]   Pulmonary capillary hemangiomatosis-like foci - An autopsy study of 8 cases [J].
Havlik, DM ;
Massie, LW ;
Williams, WL ;
Crooks, LA .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2000, 113 (05) :655-662
[13]   Pulmonary edema complicating continuous intravenous prostacyclin in pulmonary capillary hemangiomatosis [J].
Humbert, M ;
Maître, S ;
Capron, F ;
Rain, B ;
Musset, D ;
Simonneau, G .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (05) :1681-1685
[14]   DIFFERENT DISTRIBUTION OF PLEXIFORM LESIONS IN PRIMARY AND SECONDARY PULMONARY-HYPERTENSION [J].
JAMISON, BM ;
MICHEL, RP .
HUMAN PATHOLOGY, 1995, 26 (09) :987-993
[15]  
Jing XF, 1998, ARCH PATHOL LAB MED, V122, P94
[16]   FAMILIAL PULMONARY CAPILLARY HEMANGIOMATOSIS RESULTING IN PRIMARY PULMONARY-HYPERTENSION [J].
LANGLEBEN, D ;
HENEGHAN, JM ;
BATTEN, AP ;
WANG, NS ;
FITCH, N ;
SCHLESINGER, RD ;
GUERRATY, A ;
ROULEAU, JL .
ANNALS OF INTERNAL MEDICINE, 1988, 109 (02) :106-109
[17]   Monoclonal endothelial cell proliferation is present in primary but not secondary pulmonary hypertension [J].
Lee, SD ;
Shroyer, KR ;
Markham, NE ;
Cool, CD ;
Voelkel, NF ;
Tuder, RM .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (05) :927-934
[18]  
LEONE O, 2003, 3 WORLD S PULM ART H
[19]   Pulmonary veno-occlusive disease [J].
Mandel, J ;
Mark, EJ ;
Hales, CA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (05) :1964-1973
[20]   PULMONARY VASCULAR-LESIONS OCCURRING IN PATIENTS WITH CHRONIC MAJOR VESSEL THROMBOEMBOLIC PULMONARY-HYPERTENSION [J].
MOSER, KM ;
BLOOR, CM .
CHEST, 1993, 103 (03) :685-692