Difference between revisions of "Pulmonary hypertension"
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*Secondary, e.g. due to congenital heart disease (like ventricular septal defect), interstitial pulmonary fibrosis. | *Secondary, e.g. due to congenital heart disease (like ventricular septal defect), interstitial pulmonary fibrosis. | ||
==Non-secondary pulmonary hypertension== | ===Non-secondary pulmonary hypertension=== | ||
Causes:<ref name=pmid16263465>{{cite journal |author=Bush A |title=Pulmonary hypertensive diseases |journal=Paediatr Respir Rev |volume=1 |issue=4 |pages=361-7 |year=2000 |month=December |pmid=16263465 |doi=10.1053/prrv.2000.0077 |url=}}</ref> | Causes:<ref name=pmid16263465>{{cite journal |author=Bush A |title=Pulmonary hypertensive diseases |journal=Paediatr Respir Rev |volume=1 |issue=4 |pages=361-7 |year=2000 |month=December |pmid=16263465 |doi=10.1053/prrv.2000.0077 |url=}}</ref> | ||
*Primary pulmonary hypertension. | *Primary pulmonary hypertension. | ||
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*PVOD is based on case reports - it is extremely rare.<ref name=pmid3342678>{{cite journal |author=Vevaina JR, Mark EJ |title=Thoracic hemangiomatosis masquerading as interstitial lung disease |journal=Chest |volume=93 |issue=3 |pages=657-9 |year=1988 |month=March |pmid=3342678 |doi= |url=}}</ref> | *PVOD is based on case reports - it is extremely rare.<ref name=pmid3342678>{{cite journal |author=Vevaina JR, Mark EJ |title=Thoracic hemangiomatosis masquerading as interstitial lung disease |journal=Chest |volume=93 |issue=3 |pages=657-9 |year=1988 |month=March |pmid=3342678 |doi= |url=}}</ref> | ||
==Primary pulmonary hypertension== | |||
*AKA ''pulmonary plexogenic arteriopathy''.<ref name=dccpad>Lie JT, Silver MD. Diagnostic criteria of cardiovascular pathology: acquired diseases. ISBN 0-397-51630-4. PP.208-9.</ref> | *AKA ''pulmonary plexogenic arteriopathy''.<ref name=dccpad>Lie JT, Silver MD. Diagnostic criteria of cardiovascular pathology: acquired diseases. ISBN 0-397-51630-4. PP.208-9.</ref> | ||
*Like chronic pulmonary hypertension due to congenital heart disease but ''without'' the congenital heart disease.<ref name=dccpad/> | *Like chronic pulmonary hypertension due to congenital heart disease but ''without'' the congenital heart disease.<ref name=dccpad/> | ||
**Classified by ''Heath-Edwards classification'' (see below) into six grades. | **Classified by ''Heath-Edwards classification'' (see below) into six grades. | ||
==Pulmonary veno-occlusive disease (PVOD)== | |||
Features:<ref>PPP PP.393-6.</ref> | Features:<ref>PPP PP.393-6.</ref> | ||
*Clinical - gradual dyspnea +/- non-productive cough, +/- clubbing. | *Clinical - gradual dyspnea +/- non-productive cough, +/- clubbing. | ||
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DDx: chronic interstitial pneumonia. | DDx: chronic interstitial pneumonia. | ||
==Pulmonary capillary hemangiomatosis (PCH)== | |||
General: | General: | ||
*First reported in 1978 by Wagenvoort et al..<ref name=pmid730121>{{cite journal |author=Wagenvoort CA, Beetstra A, Spijker J |title=Capillary haemangiomatosis of the lungs |journal=Histopathology |volume=2 |issue=6 |pages=401-6 |year=1978 |month=November |pmid=730121 |doi= |url=}}</ref> | *First reported in 1978 by Wagenvoort et al..<ref name=pmid730121>{{cite journal |author=Wagenvoort CA, Beetstra A, Spijker J |title=Capillary haemangiomatosis of the lungs |journal=Histopathology |volume=2 |issue=6 |pages=401-6 |year=1978 |month=November |pmid=730121 |doi= |url=}}</ref> | ||
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==See also== | ==See also== | ||
*[[Medical lung diseases]]. | *[[Medical lung diseases]]. | ||
*[[Congenital heart disease]]. | |||
*[[Heart]]. | *[[Heart]]. | ||
Revision as of 02:56, 7 September 2010
Pulmonary hypertension is bad stuff that arises from heart problems and an assortment of weird stuff.
General classification
- Primary, i.e. primary pulmonary hypertension, or
- Secondary, e.g. due to congenital heart disease (like ventricular septal defect), interstitial pulmonary fibrosis.
Non-secondary pulmonary hypertension
Causes:[1]
- Primary pulmonary hypertension.
- Pulmonary embolic disease (thromboembolism, and non-thrombotic embolism).
- Pulmonary capillary haemangiomatosis (PCH).
- Pulmonary veno-occlusive disease (PVOD).
Notes:
- Some people consider PCH and PVOD to the be same thing.[2]
- Both have a poor prognosis.
- Clinically they present the same way.
- PVOD is based on case reports - it is extremely rare.[3]
Primary pulmonary hypertension
- AKA pulmonary plexogenic arteriopathy.[4]
- Like chronic pulmonary hypertension due to congenital heart disease but without the congenital heart disease.[4]
- Classified by Heath-Edwards classification (see below) into six grades.
Pulmonary veno-occlusive disease (PVOD)
Features:[5]
- Clinical - gradual dyspnea +/- non-productive cough, +/- clubbing.
- Thrombosis - small veins & venules, particularily at the interlobular septae.
- Associated with mild homogenous peripheral interstitial fibrosis.
DDx: chronic interstitial pneumonia.
Pulmonary capillary hemangiomatosis (PCH)
General:
- First reported in 1978 by Wagenvoort et al..[6]
Features:
- Proliferating and invasive capillaries.[7]
- Demonstrated by CD34 immunostaining.[2]
- Dilated capillaries[8][9] - key feature.
DDx:
- Passive congestion (PC).
- Differentiated by fact that PCH has multiple channels in alveolar wall (PC has only one).
Chronic pulmonary hypertension due to congenital heart disease
Heath-Edwards classification
Definition:[10]
- Six grades - based on intimal reaction and media of arteries and arterioles:
- Grade 1:
- Intima: no intimal reaction.
- Media: hypertrophied.
- Grade 2:
- Intima: cellular intimal reaction.
- Media: hypertrophied.
- Grade 3:
- Intima: fibrous & fibroelastic reaction + cellular intimal reaction.
- Media: hypertrophy +/- generalized dilation.
- Grade 4:
- Intima: "plexiform lesions" + fibrous & fibroelastic reaction, + cellular intimal reaction.
- Plexiform lesions = multiple channels that are dilated, assoc. with loss of elastic laminae; thought to arise at branch points due to aberant WSS.[12]
- Media: generalized dilation +/- local "dilation lesions".
- Micrographs: Plexiform lesions (ucsf.edu), Plexiform lesions (pvrireview.org).
- Intima: "plexiform lesions" + fibrous & fibroelastic reaction, + cellular intimal reaction.
- Grade 5:
- Intima: as in Grade 4.
- Media: generalized dilation + local "dilation lesions" + pulmonary hemosiderosis.
- Grade 6:
- Intima: as in Grade 4.
- Media: generalized dilation + local "dilation lesions" + pulmonary hemosiderosis + necrotizing arteritis.
- Grade 1:
Notes:
- Bolded text - defining feature.
- It is discussed here: http://www.pathology.or.kr/studygroup/cardiopulmonary/lecture/lenote/hka.htm.
See also
References
- ↑ Bush A (December 2000). "Pulmonary hypertensive diseases". Paediatr Respir Rev 1 (4): 361-7. doi:10.1053/prrv.2000.0077. PMID 16263465.
- ↑ 2.0 2.1 Lantuéjoul S, Sheppard MN, Corrin B, Burke MM, Nicholson AG (July 2006). "Pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis: a clinicopathologic study of 35 cases". Am. J. Surg. Pathol. 30 (7): 850-7. doi:10.1097/01.pas.0000209834.69972.e5. PMID 16819327.
- ↑ Vevaina JR, Mark EJ (March 1988). "Thoracic hemangiomatosis masquerading as interstitial lung disease". Chest 93 (3): 657-9. PMID 3342678.
- ↑ 4.0 4.1 Lie JT, Silver MD. Diagnostic criteria of cardiovascular pathology: acquired diseases. ISBN 0-397-51630-4. PP.208-9.
- ↑ PPP PP.393-6.
- ↑ Wagenvoort CA, Beetstra A, Spijker J (November 1978). "Capillary haemangiomatosis of the lungs". Histopathology 2 (6): 401-6. PMID 730121.
- ↑ Tron V, Magee F, Wright JL, Colby T, Churg A (November 1986). "Pulmonary capillary hemangiomatosis". Hum. Pathol. 17 (11): 1144-50. PMID 3770733.
- ↑ MC August 2009.
- ↑ PPP PP.396-7.
- ↑ 10.0 10.1 HEATH D, EDWARDS JE (October 1958). "The pathology of hypertensive pulmonary vascular disease; a description of six grades of structural changes in the pulmonary arteries with special reference to congenital cardiac septal defects". Circulation 18 (4 Part 1): 533-47. PMID 13573570.
- ↑ Jaklitsch MT, Linden BC, Braunlin EA, Bolman RM, Foker JE (June 2001). "Open-lung biopsy guides therapy in children". Ann. Thorac. Surg. 71 (6): 1779-85. PMID 11426747.
- ↑ http://pathhsw5m54.ucsf.edu/overview/vessels.html