- Open Access
In search of markers of treatment failure and poor prognosis in IPAH - the value of mosaic lung attenuation pattern on thin-section CT scans
© Novamedia srl 2010
- Received: 22 February 2010
- Accepted: 30 April 2010
- Published: 20 December 2010
Despite the development of specific therapies for pulmonary arterial hypertension (PAH) some patients fail to respond to such treatment. One of the potential reasons for the unresponsiveness to targeted therapies may be the presence of fibrous occlusion of small pulmonary veins that accompanies pre-capillary arteriopathy. This type of pathologic change is called pulmonary veno-occlusive disease (PVOD). Underdiagnosed PVOD occurs probably in 5-10% of idiopathic pulmonary hypertension (IPAH) and in a substantial proportion of PAH related to connective tissue diseases (mainly in scleroderma). A definite diagnosis of PVOD requires histological examination of lung sample, but surgical lung biopsy in pulmonary hypertension is combined with high risk of bleeding. Thus major interest is focused on a non-invasive diagnostic approach enabling early recognition of PVOD and referral for lung transplantation. The present review is focused on the radiological features suggestive of PVOD-like vasculopathy in PAH.
Alla ricerca di un marker di resistenza al trattamento e prognosi infausta nell’ipertensione polmonare idiopatica (IPAH) – il valore del pattern di attenuazione a mosaico nella TAC torace a sezioni sottili
Nonostante lo sviluppo di trattamenti specifici per l’ipertensione arteriosa polmonare (PAH) alcuni pazienti non rispondono alla terapia.
Una delle possibili ragioni può essere la presenza di un’occlusione fibrotica delle piccole vene polmonari in associazione con una arteriopatia pre-capillare. Questo tipo di alterazione è denominata malattia polmonare veno-occlusiva(PVOD). Probabilmente una PVOD non diagnosticata sottende a circa il 5-10% delle forme di ipertensione polmonare idiopatica (IPAH) ed a una quota rilevante delle forme di PAH secondarie a collagenopatie (soprattutto la sclerodermia). Per una diagnosi di certezza di PVOD è necessario l’esame istologico di un campione di tessuto polmonare, ma una biopsia polmonare chirurgica nell’ipertensione polmonare è ad alto rischio di sanguinamento. Vi è quindi un grande interesse per individuare un approccio diagnostico non invasivo che permetta un riconoscimento precoce della PVOD e l’avvio al trapianto polmonare. Questa rassegna è incentrata sugli aspetti radiologici suggestivi di una vascolopatia tipo PVOD nella PAH.
- CT scan
- idiopathic pulmonary hypertension
- mosaic lung attenuation
- pulmonary veno-occlusive disease
- malattia polmonare veno-occlusiva
- pattern di attenuazione a mosaico
- TAC torace
Updated clinical classification of pulmonary hypertension
1. Pulmonary arterial hypertension (PAH)
1.2.2 ALK1, endoglin (with or without hereditary hemorrhagic teleangiectasia)
1.3 Drugs and toxins induced
1.4 Associated with (APAH):
1.4.1 Connective tissue diseases
1.4.2 HIV infection
1.4.3 Portal hypertension
1.4.4 Congenital heart disease
1.4.6 Chronic haemolytic anemia
1.5 Persistent pulmonary hypertension of the newborn
1' Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis
2. Pulmonary hypertension due to left heart disease
2.1 Sysytolic dysfunction
2.2 Diastolic dysfunction
2.3 Valvular disease
3. Pulmonary hypertension due to lung diseases and/or hypoxemia
3.1 Chronic obstructive pulmonary disease
3.2 Interstitial lung disease
3.3 Other pulmonary diseases with mixed restrictive and obstructive pattern
3.4 Sleep-disordered breathing
3.5 Alveolar hypoventilation disorders
3.6 Chronic exposure to high altitude
3.7 Developmental abnormalities
4. Chronic thromboembolic pulmonary hypertension
5. Pulmonary hypertension with unclear and/or multifactorial mechanisms
5.1 Hematological disorders: myeloproliferative disorders, splenectomy
5.2 Systemic disorders: sarcoidosis, pulmonary Langerhans cell histiocytosis, lymphangioleiomyomatosis, neurofibromatosis, vasculitis
5.3 Metabolic disorders: glycogen storage disease, Gaucher disease, thyroid disorders
5.4 Others: tumoral obstruction, fibrosing mediastinitis, chronic renal failure on dialysis
The common feature for group 1, called pulmonary arterial hypertension (PAH), is pre-capillary pulmonary arteriopathy. This group includes: idiopathic PAH, heritable PAH, and PAH associated with: connective tissue diseases (CTD), congenital heart diseases (CHD), systemic-to-pulmonary shunts, portal hypertension, HIV, use of drugs or anorexigens and many other conditions listed in Table 1.
The two entities: pulmonary veno-occlusive disease (PVOD) and pulmonary capillary hemangiomatosis (PCH) were removed from group 1 to a separate group 1', due to the different pathomechanism of pulmonary hypertension (pathologic changes localized in capillaries and in small venules, causing capillary hypertension and secondary arterial hypertension).
Group 2 is composed of PH as a consequence of left heart pathology.
Group 3 encompasses PH related to pulmonary disease leading to capillary destruction and/or hypoxic pulmonary vasoconstriction.
Group 4 consists of PH due to chronic thromboembolic pulmonary disease (CTEPH).
Group 5 is composed of PH with unclear or multi-factorial mechanisms.
The routine diagnostic procedures involved in the differential diagnosis of PH consist of physical examination, blood and serologic tests, chest radio gram, echocardiographic study, chest computerized tomography (CT) scan, ventilation-perfusion scintigraphy and pulmonary function tests (PFT) [4, 5]. Right heart catheterization is not only obligatory for confirmation of PH, but it is also a very important tool in the differential diagnosis of other forms of PH [4, 5].
Thus PH related to parenchymal lung diseases and chronic obstructive pulmonary disease (COPD) is diagnosed when significant PFT abnormalities +/- pathologic parenchymal changes in lung CT scan are found. In the case of PH in the course of obstructive sleep apnea, pathologic polysomno graphy is diagnostic.
PH related to left heart diseases (venous, post-capillary PH) is diagnosed in the case of left heart myocardial or valvular disease with increased PCWP.
CTEPH is diagnosed in those patients with PH who present segmental hypoperfusion areas on lung per-fusion scan (scintigraphy with high probability of pulmonary embolism). The majority of these patients have had an episode of symptomatic venous thromboembolic disease in their medical history, and in some of them intravascular filling defects can be demonstrated on chest CT angio graphy or arteriography .
PAH is diagnosed after the exclusion of the above-mentioned, most frequent causes of PH. It is the most extensively investigated group due to the possibility of specific therapeutic approaches: prosta cyclin derivatives, endothelin receptor antagonists and phosphodiesterase-5 inhibitors [5–8]. Prolonged specific treatment of PAH is combined with a significant improvement of functional class, increase of exercise tolerance measured by the 6 minute walking test (6 MWT), a decrease in serum biomarkers of myocardial injury and decompensation (troponin, BNP, NT-proBNP) and an improvement of pulmonary hemodynamics [5, 9–11]. The results of a large meta-analysis involving 3,140 patients from 21 studies, presented recently by Galié et al. , indicate also a positive prognostic influence of specific treatment in PAH (43% reduction in mortality over 14.3 weeks).
Despite progress in specific treatment of PAH, there are some patients in whom the treatment is ineffective or even combined with a worsening of clinical symptoms.
This happens most frequently in PVOD/PCH, where the presence of capillary and post-capillary occlusion causes an increase of trans-capillary pressure with signs and symptoms of pulmonary congestion . Underdiagnosed PVOD occurs probably in 5-10% of IPAH . The clinical presentation of such cases may be indistinguishable from IPAH, excepting for a rapid development of pulmonary edema after administration of vasodilators. Harch et al.  examined lung specimens available from autopsy or explantation in 14 patients with clinically diagnosed PAH who had failed to respond to medical therapy and found PVOD in 86% of them and "arterial-only" PAH in the remaining 14%. Montani et al.  described the development of pulmonary edema (mostly with continuous intravenous epoprostenol, but also with oral bosentan and calcium channel blockers) in 7/16 patients with pathologically proved PVOD (43.8%) at a median of 9 days after treatment initiation.
The definite diagnosis of PVOD/PCH requires a pathologic examination of lung tissue. Lung biopsy is contraindicated in the majority of patients with PH, due to the possibility of life-threatening bleeding [15, 16]. Thus pathologic material is usually obtained from explanted lung or - unfortunately during autopsy.
In PVOD fibrous venules remodeling with secondary capillary proliferation, pulmonary hemosiderosis, interstitial edema and lymphatic dilatation is found [17, 18]. Pulmonary and mediastinal lymph nodes enlargement due to venous congestion and veno-lymphatic shunts has been described by Montpréville et al. .
In PCH, capillary proliferation develops, either as the isolated pathology or, more frequently, as a reaction to increased venous pressure due to venous occlusion. Thus most pathologists use the name PVOD/PCH for such pathology [17, 18]. Despite the occurrence of secondary pre-capillary arteriopathy in some PVOD/PCH cases, no complex lesions in pulmonary arteries are observed [17, 18].
Poor results of specific treatment may be also observed in PAH related to CTD [20–22]. Despite some recently reported therapeutic achievements in PAH-CTD [23–25], the results are worse than in IPAH. Dorfmuller et al.  described recently fibrous remodeling of the pulmonary venous system in PAH-CTD. This phenomenon may explain why these patients are less prone to respond to specific PAH treatment compared with IPAH. The authors suggest a clinically relevant hemodynamic effect of post-capillary occlusion in a setting of PAH-CTD, with PVOD-like pathology. PVOD-like pathology was described in PAH-CTD also by Overbeck et al.  and in the course of fatal granulomatous angiitis by Dwyer et al. .
The search for clinical markers of PVOD/PCH drew attention to the presence of lung pathology seen occasionally on CT scans in PAH.
In the majority of IPAH patients the only radiological abnormality seen on CT scans are the signs of pulmonary hypertension such as dilatation of pulmonary artery, pulmonary artery/aorta diameter > 1 and right ventricular enlargement . Nevertheless some investigators have noted the presence of mosaic attenuation on HRCT scans in IPAH patients.
Stern et al.  made an effort to categorize the diseases leading to mosaic pattern of lung attenuation. Three categories of lung disease are known to cause a mosaic pattern of lung attenuation on CT scan: small airways diseases, pulmonary vascular diseases and infiltrative lung diseases.
The mosaic pattern of lung attenuation caused by small airways diseases is a result of air trapping. This condition is recognized on CT scans obtained at full expiration. The mosaic pattern of lung attenuation caused by primary vascular disease is caused by regions of hyperemic lung (with higher attenuation) adjacent to oligemic regions of the lung (with lower attenuation). Mosaic attenuation due to vascular disease and due to small airways disease may produce a similar CT picture performed at inspiration - with decrease of size and number of vessels in lucent parts of the lung compared with the regions with higher attenuation. Nevertheless no air trapping is seen on expiratory CT in the case of vascular disease.
The third cause of mosaic lung attenuation is an infiltrative lung disease, with areas of ground-glass attenuation due to interstitial or air space infiltrates, or both. In this condition no air trapping is seen on expiratory CT but the number and size of vessels in the areas of ground glass attenuation is similar to the areas of normal lung parenchyma.
The heterogeneity of perfusion in PAH is less prominent than in CTEPH, due to the smaller caliber of occluded vessels and more dispersed nature of the disease. Thus in the majority of PAH patients heterogeneity of lung perfusion is not seen. Nevertheless in some IPAH patients inhomogeneity of lung parenchyma is recognized but the mechanism involved in this pathology and the clinical significance of such finding is not clear.
Resten et al.  analyzed HRCT in 12 IPAH patients with epoprostenol therapy failure (group 1) and compared them to 61 patients who improved during such therapy (group 2). Frequency of ground-glass opacities in groups 1 and 2 was, respectively, 83% and 38%. The authors divided ground-glass opacities into two categories: class I - poorly defined nodular opacities ranging in diameter from a few millimeters to 1 centimeter with centrilobular distribution, and class II - pan-lobular distribution of geographic regions of lung attenuation with relatively well defined borders. Class I opacities were found more frequently in group 1 than in group 2 (61% and 21%, respectively). The frequency of class II opacities was similar in both groups (25% and 16% respectively). Thus only the presence of class I opacities correlated with the failure of epoprostenol therapy. The other parameters correlated with epoprostenol failure were: thickened interlobular septa, mediastinal lymphadenopathy and the presence of pericardial effusion. The results of post-mortem examination were available in 6 patients from group 1 and revealed the presence of PVOD or PCH in all of them. The authors concluded that the presence of poorly defined centrilobular opacities in combination with thickened septal lines, pleural or pericardial effusion and/or adenopathy in the patients with IPAH should raise a suspicion of PVOD or PCH.
The occurrence of centrilobular nodules in 25% of PAH patients was also described by Nolan et al. , who found the presence of cholesterol granulomas in them on pathologic examination. The mechanism of development of such granulomas could be related, according to the authors, to the degradation of excess of surfactant or to recurrent pulmonary hemorrhage. The nodules described by Nolan et al.  in PAH were an isolated finding, with no septal lines or lymphadenopathy.
PVOD/PCH with the pathological changes seen in small venules and capillaries produces the radiological signs of pulmonary congestion and impaired lymphatic drainage. The typical radiological changes described on CT scans in PVOD represent the combination of septal lines, lymphadenopathy and pleural effusion. Many authors have also noted the presence of poorly defined centrilobular nodular opacities in PVOD.
Resten et al.  analyzed radiological features of pathologically confirmed PVOD in 15 patients and compared them with radiological features of 15 PAH patients. He found the presence of ground-glass opacities in 87% of PVOD and in 33% of PAH (p = 0.003), septal lines in 93% of PVOD and 13% of PAH (p < 0.0001) and lymph nodes enlargement in 80% of PVOD and 0% of PAH (p < 0.0001). The presence of pleural effusion, noted in 23% of PVOD and 13% of PAH, was not helpful in the differential diagnosis. The authors concluded that pleural effusion is a less specific sign of PVOD and should be regarded as characteristic only in the presence of other radiological PVOD features. This observation was confirmed by data reported by Tang et al. , who demonstrated pleural effusion in 25% of IPAH, mostly due to right heart failure. The patients with pleural effusion had significantly higher mean right atrial pressure (mRAP) than the remaining patients (16.0 ± 6.8 mm Hg and 8.8 ± 5.5 mm Hg respectively). The majority of effusions were small and right sided.
The type of ground-glass opacities found by Resten et al.  was either centrilobular or pan-lobular. Centrilobular nodules were more characteristic of PVOD; nevertheless they appeared occasionally also in PAH.
It is not clear whether centrilobular nodules seen in PVOD represent a venopathy or alveolar consolidations due to lung congestion. Cassart et al.  described a complete resolution of ground-glass opacities in native lung 84 days after single lung transplantation in PVOD. This finding might support the theory of centrilobular nodules as a sign of pulmonary congestion in the presence of impaired outflow on the level of small pulmonary veins.
Dufour et al.  described small, centrilobular, poorly circumscribed nodular opacities in combination with thickening of interlobular septa in 2 patients with PCH and 2 patients with PVOD (biopsy proven). All these patients developed fatal pulmonary edema after treatment with intravenous epoprostenol.
The combination of centrilobular ground-glass opacities, septal lines and lymph nodes enlargement on lung CT scan had, according to Montani et al. , a 75% sensitivity and 85% specificity for detection of PVOD. Nevertheless the absence of such changes or the presence of only one radiological abnormality could not rule out PVOD.
El-Gabaly et al.  reported a case of PCH confirmed by open lung biopsy presenting on HRCT scans with numerous ill-defined centrilobular micronodular densities affecting both lungs, with no other radiological abnormalities. Isolated centrilobular ground-glass opacities were described recently by Iwaki et al.  in a 52-year-old female with biopsy-proven PVOD.
Differential diagnosis of idiopathic PAH and idiopathic PVOD
BMPR2 mutations 10-40%
Cases of BMPR2 mutation
F:M = 2
F:M = 1
More frequent than in IPAH
Pulmonary function tests
Normal (possible mild restrictive)
Normal (possible mild restrictive)
DL CO and DL CO /VA
Reduced, lower than IPAH
PaO 2 at rest
Reduced, lower than IPAH
Frequent abnormalities: Centrilobular ground-glass opacities Septal lines Lymph node enlargement
Possible occult alveolar hemorrhage
Acute NO testing
Positive: predictive of CCB response and better prognosis
Not a predictor of CCB response (risk of pulmonary edema after initiation of CCB)
Response to PAH therapy
Improved hemodynamics, functional status and outcome
PVOD may deteriorate with a risk of pulmonary edema
The other important feature of PVOD is the presence of occult alveolar hemorrhage. This observation was made by Rabiller et al. , who found in bronchoalveolar lavage a higher percentage of hemosiderin laden macrophages in PVOD compared to IPAH.
The reasons for a worse hypoxemia in PVOD than expected from PAP levels are: pulmonary edema, alveolar hemorrhage and overall more extensive obliteration of the pulmonary vascular bed. Montani et al.  found no significant differences in hemodynamic parameters between PVOD and IPAH. PCWP is not greater in PVOD compared to IPAH, as it reflects the pressure in the pulmonary veins with a caliber similar to the pulmonary artery branch where the catheter is inserted and the occlusion maneuver performed, whilst the caliber of small veins and venules affected by PVOD is smaller.
Holcomb et al.  presented data concerning poor prognosis in PVOD: the 1-year mortality rate may be as high as 72%. Montani et al.  found the mean time from diagnosis to death or lung transplant in PVOD to be 11.8 ± 16 months, which was significantly worse than in IPAH (42.3 ± 29.9 months). The worse outcome of PVOD patients is probably related to the development of pulmonary edema either as part of the natural course of the disease or as precipitated by specific pulmonary vasodilator therapies. Due to the worse prognosis in PVOD patients and no evidence of effective pharmacotherapy, it is important to consider lung transplantation early in the course of the disease.
In summary, PVOD/PCH is a disease difficult to diagnose, in some cases presenting with a wide spectrum of radiologic abnormalities, but in many others indistinguishable from IPAH until the development of signs of pulmonary congestion in the course of treatment with vasodilators. The presence of ill-defined centrilobular nodules on lung HRCT scan in IPAH especially in combination with thickened septal lines and/or lymphadenopathy should draw attention to the possibility of a PVOD-like pathology. Targeted therapies should be applied with caution in such patients.
Lack of effect of targeted therapy should be a reason for early referral for lung transplantation.
None of the authors has any conflict of interest to declare in relation to the subject matter of this manuscript.
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