Pulmonary Medicine

Pulmonary Medicine / 2015 / Article

Research Article | Open Access

Volume 2015 |Article ID 230846 | https://doi.org/10.1155/2015/230846

Kay Maeda, Yoshikatsu Saiki, Shigeo Yamaki, "In Situ Thrombosis of Small Pulmonary Arteries in Pulmonary Hypertension Developing after Chemotherapy for Malignancy", Pulmonary Medicine, vol. 2015, Article ID 230846, 6 pages, 2015. https://doi.org/10.1155/2015/230846

In Situ Thrombosis of Small Pulmonary Arteries in Pulmonary Hypertension Developing after Chemotherapy for Malignancy

Academic Editor: Charlie Strange
Received08 Nov 2014
Revised11 Jan 2015
Accepted11 Jan 2015
Published27 Jan 2015


A few reports have provided histopathological insight into pulmonary hypertension developing after antitumor chemotherapy. In general, plexogenic pulmonary arteriopathy is a commonly observed finding in patients with severe pulmonary hypertension. We herein report a novel pathological finding that may characterize the histopathological change occurring in patients with pulmonary hypertension after chemotherapy for malignancy. Lung biopsy or autopsy was performed in 7 patients with pulmonary hypertension that developed during or after chemotherapy between 2006 and 2013 to examine the pulmonary vascular changes or to determine the cause of death. Pathological findings included in situ thrombosis in the small pulmonary arteries in 4 of 7 patients. In 2 of 4 patients, pulmonary hypertension was controlled by anticoagulants and antithrombotic agents. One patient who had organized thrombi attained spontaneous remission with oxygen therapy. The other patient died of sudden cardiopulmonary arrest during chemotherapy. Autopsy showed complete occlusion of the peripheral small pulmonary arteries and veins by thrombi. These results demonstrate that in situ thrombosis in the small pulmonary arteries could cause pulmonary hypertension after chemotherapy.

1. Introduction

Pulmonary hypertensive disease can develop after chemotherapy for various malignant tumors and becomes lethal in immunocompromised patients. A few case reports have implicated a probable relationship between chemotherapy and subsequent pulmonary hypertension (PH) [13]. However, there have been few reports on pathological findings that are characteristic to this devastating sequela [4].

To date, we have performed a significant number of lung biopsies for diagnoses of severe PH associated with congenital and acquired heart diseases [5]. We reported distinctive pulmonary vascular changes even in relatively rare diseases associated with PH, such as chronic thromboembolic pulmonary hypertension (CTEPH), pulmonary venoocclusive disease (PVOD), idiopathic pulmonary arterial hypertension (IPAH), and portosystemic venous shunt (PSVS) [610]. In patients with severe PH, plexogenic pulmonary arteriopathy generally develops in the small pulmonary arteries [11].

In the present study, we demonstrate that in situ thrombosis in the small pulmonary arteries is one of the causative mechanisms for PH associated with chemotherapy.

2. Materials and Methods

Between 2006 and 2013, 7 patients who developed PH after chemotherapy for various malignancies were histopathologically examined at our research institute. Lung biopsies (3 cases) and autopsies (4 cases) were conducted to investigate the cause of unexplained PH after chemotherapy or to determine the cause of death, in detail, in terms of histopathological characteristics. The Heath-Edwards (HE) classification was used to assess the arterial changes [12].

Lung tissue was obtained from a lobe of the lung and was fixed in 10% formalin. In each case, 30 semiserial histological sections at 50 μm intervals, each 3 μm thick, were prepared as previously described [5]. Then, modified Elastica–Goldner staining was performed for the histopathological analysis [13]. All protocols were conducted in compliance with the Helsinki Declaration. They were also approved by the Ethical Committee of the Japanese Research Institute of Pulmonary Vasculature and each referred hospital. Informed consent was obtained from all patients.

3. Results

The clinical and pathological characteristics of patients who developed PH after chemotherapy are presented in Table 1. Most patients (6/7) were young children (2–6 years old), including 4 lethal cases. The time interval between chemotherapy and the onset of PH varied from a few days to years. Histopathological analysis revealed that the cause of unexplained PH was in situ thrombosis in the small pulmonary arteries in 4 of 7 patients (cases 1–4). In the other 3 patients (cases 5–7), the pathological diagnoses were PVOD, IPAH, and plexogenic arteriopathy. In case 3, congenital partial protein C deficiency, which causes a clotting disorder, was detected after lung biopsy as the result of intensive examination to investigate the cause of thrombi. However, the others (cases 1, 2, and 4) had no thrombotic diathesis. The clinical findings of patients (cases 1–4), who were pathologically diagnosed with in situ thrombosis in small pulmonary arteries, are shown in Table 2.

CaseAge, sexNeoplasmTreatment for neoplasmPeriod from chemotherapy to PH onsetClinical diagnosis cause of deathPathological findingsLung specimen

146, MMalignant lymphomaSurgical resection +
8 yearsIPIn situ thrombosis of SPA and veinsBiopsy
26, FNBSurgical resection +
AutoPBSCT () + high-dose chemotherapy
7 daysIP, PVODIn situ thrombosis of SPA and veinsBiopsy
32, FALLUmbilical cord blood transplant () + high-dose chemotherapy10 daysPAH,
Congenital protein C deficiency
In situ thrombosis of SPABiopsy
42, MRMSChemotherapy +
Proton therapy
During chemotherapyHepatic venoocclusive disease unknownIn situ thrombosis of SPA and veinsAutopsy
55, MBurkitt’s
ChemotherapyDuring chemotherapyPVOD refractory right HF]PVODAutopsy
63, MMBSurgical resection +
9 monthss/o PAH, PVOD
IPAH, IPAutopsy
72, FAMLAllogeneic bone marrow transplant + high-dose chemotherapy2 monthss/o PVOD, cGVHD IPPlexogenic arteriopathy, IPAutopsy

ALL = acute lymphocytic leukemia; AML = acute myelogenous leukemia; AutoPBSCT = autologous peripheral blood stem cell transplantation; cGVHD = chronic graft versus host disease; F = female; HF = heart failure; IP = interstitial pneumonia; IPAH = idiopathic pulmonary arterial hypertension; M = male; MB = medulloblastoma; NB = neuroblastoma; PAH = pulmonary arterial hypertension; PH = pulmonary hypertension; PVOD = pulmonary venoocclusive disease; RMS = rhabdomyosarcoma; SPA = small pulmonary arteries.

CaseClinical symptomsComputed tomographyEchocardiographyPAGClinical outcome

1DOEGround-glass opacity
Diffuse patchy nodular interstitial opacity
Normal Tapering vascular shadow of both upper lungs, mPAP = 30 mmHgOxygen therapyimproved
2Polypnoea, hypoxemiaGround-glass opacity
Pleural effusion
mPAP = 70–75, 55 mmHg (under NO),
Diureticssevere PHNO, PDE5i, PGI2anticoagulantsimproved
3DOE, hypoxemia, polypnoea, Ground-glass opacitymPAP = 40–50 mmHgNO, PDE5i, PGI2anticoagulants, antithrombotic drugsimproved
4Hypoxemia, sudden chest-abdominal painmPAP = 50–55 mmHgOxygensudden cardiopulmonary arrest (death)

DOE = dyspnea on exertion; mPAP = mean pulmonary artery pressure; PAG = pulmonary angiography; PDE5i = cGMP-specific phosphodiesterase type 5 inhibitor; PGI2 = prostaglandin I2; PH = pulmonary hypertension; RVH = right ventricular enlargement.

A 46-year-old man (case 1) underwent surgery and chemotherapy for primary testicular malignant lymphoma at the age of 38 years and remained in remission after treatment. He began to experience shortness of breath on exertion and was hospitalized due to suspicion of diffusive lung disease. Detailed examination showed no evidence of cancer recurrence. Computed tomography of the chest demonstrated ground-glass opacity. No myocardial disease was noted on the echocardiogram. Right catheterization showed tapering vascular shadows of both upper lungs, with a mean pulmonary artery pressure (PAP) of 30 mmHg. Transbronchial lung biopsy revealed mild inflammatory cell infiltration but did not yield a definite diagnosis. Therefore, video-assisted thoracic surgery was performed. Histopathology revealed long-term and extensive in situ thrombosis in the small pulmonary arteries (Figure 1(a)) and pulmonary veins (Figure 1(b)). Both the small pulmonary arteries and veins exhibited recanalization of organized fibrotic thrombi, with the lumen separated into several channels. Some small pulmonary arteries (>100 μm in diameter) showed luminal narrowing and occlusion by longitudinal smooth muscle (Figure 1(c)). There was mild inflammatory cell infiltration, but no evidence of vasculitis. Laboratory data confirmed the absence of vasculitis syndrome or coagulation disorder. The respiratory symptoms gradually improved with oxygen therapy.

A 6-year-old girl (case 2) presented with abdominal distention and abdominal pain. A biopsy specimen of the abdominal wall showed primary right adrenal neuroblastoma. Therefore, chemotherapy for neuroblastoma was initiated according to the protocol of the inpatient facility. After the fourth course of chemotherapy, tumorectomy was performed, followed by autologous peripheral blood stem cell transplantation (auto-PBSCT) and high-dose chemotherapy. Soon after completion of the second auto-PBSCT and high-dose chemotherapy, the patient exhibited polypnea and hypoxemia. Chest radiographic examination revealed moderate pleural effusion. As assessed by echocardiography, mean PAP was 40 mmHg. Hypoxia was improved by the administration of diuretics. However, 1 week later, the patient exhibited polypnea, tachycardia, aggravated hypoxemia, and chest pain. Echocardiography showed PH (mean PAP = 70–75 mmHg) and right ventricular enlargement. Mean PAP decreased to 55 mmHg under nitric oxide (NO) inhalation but increased again after NO withdrawal, despite the administration of sildenafil and epoprostenol. Therefore, lung biopsy was performed for suspected PVOD. The small pulmonary arteries (>150 μm in diameter) showed no intimal proliferation but severe medial thickening (HE classification: I). Pathological findings revealed that small pulmonary arteries and veins (<30–50 μm in diameter) were almost completely occluded by newly formed thrombi not yet organized (Figures 2(a)2(c)). The lung parenchyma presented atelectasis and cellular thickening of the alveolar wall. The patient is currently followed-up with additional administration of anticoagulants.

A 2-year-old girl (case 3) was diagnosed with acute lymphocytic leukemia (ALL) at the age of 5 months. She received high-dose chemotherapy and umbilical cord blood transplants. After the second transplant, the patient had a documented PH crisis at the age of 22 months. The respiratory symptoms were effectively relieved by NO inhalation, followed by sildenafil and beraprost administration. Echocardiography showed PH (mean PAP = 40–50 mmHg), without any myocardial disease. Therefore, PAH was suspected based on the clinical findings. Lung biopsy was performed to verify the diagnosis. Microscopically, the small pulmonary arteries showed mild medial thickening but no intimal proliferation (HE classification: I). However, thrombi at varying stages were found in almost all peripheral small-sized pulmonary arteries (Figure 3(a)). Most thrombi were still in the process of formation (Figure 3(b)). In contrast, the pulmonary veins and respiratory system appeared normal. The detailed examination to investigate the cause of these thrombi was carried out based upon the above described lung biopsy findings, and partial congenital protein C deficiency was detected. PH was successfully controlled with anticoagulants and antithrombotic agents.

A 2-year-old boy (case 4) with rhabdomyosarcoma started receiving chemotherapy at the age of 17 months, and he developed hepatic venoocclusive disease during treatment. At the age of 24 months, he became dyspneic with hypoxemia. Mild PH was detected on the electrocardiogram and echocardiogram. After a few weeks of oxygen therapy, he experienced sudden chest-abdominal pain and died of sudden cardiopulmonary arrest at the hospital at the age of 26 months. Postmortem examination of the lungs was performed to determine the cause of death. The small pulmonary arteries (>200 μm in diameter) showed moderate medial thickening without intimal lesion (HE classification: I). Some small pulmonary arteries (<100 μm in diameter) and pulmonary veins showed intimal fibrous proliferation (Figure 4). They were considered to be thrombi because of the eccentric intimal thickening. Small peripheral pulmonary arteries (<50 μm in diameter) showed complete occlusion by thrombi.

4. Discussion

This is the first study reporting in situ thrombosis in the small pulmonary arteries of patients who developed PH after chemotherapy. In contrast, several studies have reported PH due to PVOD after stem cell transplantation or chemotherapy [13]. We also diagnosed in 1 patient (case 5) that the cause of unexplained PH developing after chemotherapy was PVOD [4]. The histopathology of PVOD typically shows extensive occlusion of pulmonary veins by intimal fibrosis [14] in the form of concentric layers [6, 7]. The present cases (cases 1–4) exhibited a distinct pattern of thrombosis in pulmonary veins and small pulmonary arteries characterized by localized and eccentric intimal fibrosis. In addition, the fibrosis was associated with recanalization of the organized thrombi by separating the lumen into several channels. In contrast, plexogenic pulmonary arteriopathy, which is typically seen in PH patients, was hardly seen in all patients with in situ thrombosis in the small pulmonary arteries even with high PAP readings.

In situ thrombosis in the small pulmonary arteries is difficult to diagnose from clinical examination due to nonspecific complaints and from laboratory data. Computed tomography typically shows diffuse ground-grass opacities, patchy pulmonary opacity, atelectasis, and pleural effusion. Even with these diagnostic radiological findings, it is difficult to distinguish in situ thrombosis from other pathological conditions that can exhibit similar symptoms, such as PVOD and interstitial pneumonia. In cases 5–7, histopathological examination identified that the causes of PH were PVOD, IPAH, and interstitial pneumonia, whereas clinical findings in these cases were not distinguishable from those with in situ thrombosis. When patients undergoing antitumor chemotherapy present unexplained PH, lung disease and myocardial dysfunction should be ruled out, whereas PVOD and in situ thrombosis should be considered as differential diagnoses. Considering these facts, lung biopsy is necessary for accurate diagnosis for some patients with unexplained PH. In addition, thrombogenic factors should be investigated because some patients may develop thrombotic diathesis [15], as in case 3.

Patient 1 had mild symptoms, likely because the thrombi had developed over several years. Microscopically, organized thrombi with recanalization were found in small pulmonary arteries and veins. The direct cause of PH might be respiratory diseases, because longitudinal smooth muscles appeared under hypoxia. Therefore oxygen therapy was effective in this case. The background of organized fibrotic thrombi, which seem to have been formed a few years previously, might accelerate the bloodstream aggravation in pulmonary circulation, although the symptom was not recognized at the time of thrombosis formation. In cases 2 and 3, anticoagulants and antithrombotic agents were effective treatments for in situ thrombosis. In these cases, sudden PH resistance to pulmonary vasodilators including NO occurred, which indicated that thrombi were forming at that moment. Incidentally, histopathology revealed that small pulmonary arteries were almost completely occluded due to forming or newly formed thrombi. Thus, this wave of new thrombi caused PH to progress rapidly. In such cases, anticoagulants and antithrombotic agents have played a crucial role in survival. Interestingly, in situ thrombosis in small pulmonary arteries is one of the pathological features of PSVS [7]. These patients with PSVS responded very well to prostaglandin E1 treatment. This study suggests that prostaglandin E1 might be an effective therapy for in situ thrombosis in the small pulmonary arteries. Possible hazard to institute anticoagulation and antithrombotic therapy may include lung hemorrhage in the presence of PVOD, which can be avoided by accurate diagnosis with lung biopsy. The most efficient therapy for PVOD is, in fact, currently lung transplant. In contrast, in situ thrombosis can possibly be treated by pharmacotherapy. Regardless, initiation of treatment should not be delayed to avoid a fatal outcome as in case 4. As early diagnosis and treatment is crucial for this disease, clinicians should keep in mind that in situ thrombosis may induce the development of PH. The lung biopsy is currently the sole diagnostic method to identify in situ thrombosis in the small pulmonary arteries.

These studies apparently have significant limitations. First, this report is consisted of small series of selected patients. However, it should be noted that in situ thrombosis in the small pulmonary arteries was detected as the possible cause of PH after chemotherapy in 4 of 7 patients. Secondly, assessment of lung biopsy was carried out only once for each patient; therefore, serial changes could not be elucidated. The precise pathogenesis of in situ thrombosis is small pulmonary arteries still remains unknown.

5. Conclusions

The present study demonstrates that in situ thrombosis in the small pulmonary arteries is one of the causative mechanisms for PH developing during chemotherapy. Further research is required to elucidate the pathogenesis of PH after chemotherapy.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


The authors are grateful to the following cardiovascular institutes in Japan for the supply of materials: Departments of Pediatric Hematology and Oncology and Pediatric Cardiology, at the Okinawa Prefectural Nanbu Medical Center and Children’s Medical Center; Department of Respiratory Medicine at the Miyagi Cardiovascular and Respiratory Center; Department of Pediatrics at the Tsukuba University Hospital; Department of Cardiology at the Kanagawa Children’s Medical Center; Department of Pediatrics at the Miyazaki University Hospital.


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Copyright © 2015 Kay Maeda et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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