Evaluation of Six Patients with Pulmonary Carcinosarcoma with a Literature Review
The Scientific World Journal
Volume 2012, Article ID 167317, 5 pages
doi:10.1100/2012/167317
The cientificWorldJOURNAL
Review Article
Evaluation of Six Patients with Pulmonary Carcinosarcoma with
a Literature Review
Sinem Nedime Sökücü,1 Celalettin Kocatürk,2 Nur Ürer,3 Yaşar Sönmezoğlu,2 Levent Dalar,1
Levent Karasulu,1 Sedat Altın,1 and Mehmet Ali Bedirhan2
1 Department of Pulmonology, Yedikule Chest Disease and Thoracic Surgery Training and Research Hospital, Zeytinburnu,
34760 İstanbul, Turkey
2 Department of Thoracic Surgery, Yedikule Chest Disease and Thoracic Surgery Training and Research Hospital, Zeytinburnu,
34760 İstanbul, Turkey
3 Department of Pathology, Yedikule Chest Disease and Thoracic Surgery Training and Research Hospital, Zeytinburnu,
34760 İstanbul, Turkey
Correspondence should be addressed to Sinem Nedime Sökücü,
Received 11 October 2011; Accepted 2 January 2012
Academic Editors: E. Briasoulis, B. L. Lum, A. Paulino, and G. Storme
Copyright © 2012 Sinem Nedime Sökücü 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.
Background. Carcinosarcoma of the lung is a rare malignant neoplasm. We evaluated the diagnosis and treatment of six
carcinosarcoma cases, including a synchronous tumour and a solitary pulmonary tumour, along with the clinical and histological
features and survival times. Methods. From a retrospective analysis of 1076 non-small-cell lung cancer resections performed
between January 1996 and January 2011, six patients (0.5%) with pulmonary carcinosarcoma (all males; mean age 58 years; range
53–66) who underwent surgical treatment were studied. Results. The mean tumour pathological T diameter was 7.2 cm (median
6 cm, range 3–14.5 cm). Only one patient was diagnosed with carcinosarcoma preoperatively. The clinical presentation and tumour
localisations differed. The operations performed were a lobectomy (n = 4), pneumonectomy (n = 1), and bilobectomy (n = 1).
Histologically, the epithelial characteristics of the tumours were consistent with squamous cell carcinoma in most of the patients. A
complete resection was performed in all six patients. No mortality occurred in the early postoperative period. The median survival
time was 9 (3–25) months. Conclusion. The preoperative diagnosis of carcinosarcoma of the lung is difficult due to the composition
of the different histopathological structures. Complete surgical resection is the treatment of choice for pulmonary carcinosarcoma,
although further studies are needed.
1. Introduction
2. Material and Method
Pulmonary carcinosarcoma (PCS) is a rare tumour in humans [1, 2]. It was first defined by Kika et al. in 1908 as
a poorly differentiated non-small-cell carcinoma containing
a component with sarcoma or sarcoma-like features [3]. It
accounts for 0.3 to 1% of all pulmonary cancers, and its
clinical characteristics, preoperative diagnostic methods, and
prognostic factors are still not completely understood [4].
Pulmonary carcinosarcomas occur predominantly in elderly
men and middle-aged smokers [5]. This study evaluated the
results of six cases who underwent surgery for PCS.
This was a retrospective study of six patients who underwent
surgery for pulmonary tumours in our chest surgery clinic
between January 1996 and January 2011 and who had a postoperative diagnosis of PCS. The patients were evaluated in
terms of their age, gender, symptoms, diagnostic approaches,
surgical methods, and followup findings.
All of the patients underwent routine laboratory studies,
respiratory function tests, electrocardiography, chest X-ray,
computed tomography (CT) of the thorax, brain CT or
magnetic resonance imaging (MRI), abdominal ultrasound,
2
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Table 1: Characteristics of the patients.
Patient
Age
Cigar (pack
years)
Symptoms
Endobronchial
Component
Localization
Diameter (cm)
CT/surgical
Preoperative
diagnosis
1
63
90
Cough
hemoptysis
Yes
Right lower lobe
3/3
NSCLC
(epidermoid)
2
66
40
Chest pain,
Hemoptysis
Cough
Yes
Right central
8/10
NSCLC
with
neuroendocrine
differantiation
3
54
60
Hemoptysis
Chest pain
Cough
No
Right hiler
intermediate
Bronch
5/6,5
Carcinosarcoma
4
53
50
Hemoptysis
Chest pain
Cough
No
Left lower lobe
10/14,5
NSCLC
5
55
30
—
No
Left upper lobe
3/3,7
None
40
Chest pain
Dyspnea
No
Left lower lobe
3,7/5,5
NSCLC
6
56
NSCLC: Non-small-cell lung carcinoma.
Figure 1: Chest X-ray of a patient showing a mass lesion located left hiler localization.
and bronchoscopy. Three patients underwent positron emission tomography (PET)-CT. In the preoperative period,
one patient without a cancer diagnosis was suspected of
having lung cancer, and one patient had a diagnosis of
carcinosarcoma, whereas the other four patients were diagnosed with non-small-cell lung cancer (NSCLC). The
patient who had a preoperative diagnosis of carcinosarcoma
had an endobronchial component and was diagnosed by
bronchoscopy. The mediastinal lymph nodes were evaluated
by mediastinoscopy in all but one patient. A standard posterolateral thoracotomy incision and intraoperative staging
were done in all patients. Complete resection was done in
all patients. All of the tumours were staged postoperatively
according to the seventh international TNM staging system.
The diagnosis was verified immunohistochemically.
All patients underwent clinical and radiological followup for a median of 7.5 (range 3–25) months. All patients were
assessed quarterly for the first 2 years with a history, physical
examination, and chest X-ray. Laboratory tests and advanced
radiological methods were requested if there were any symptoms. Additionally, all patients or the families were asked by
phone when the study was performed and asked about any
signs of recurrence or complications.
The statistical analysis was done using SPSS ver. 11.5.
Descriptive analyses and Kaplan-Meier survival analysis were
used.
3. Results
All six patients were male and heavy smokers (mean 52
packs/year (median 45, range 30–90)), with a median age
of 56 (range 53–66) years. The most common presenting
symptom was cough (Table 1).
Two of the tumours were located peripherally, three were
located centrally (Figure 1), and the sixth had components in
both areas. The diagnosis was made by fine-needle aspiration
biopsy in two patients and by fibre optic bronchoscopy in
three patients. Three of the six patients underwent PETCT. In these patients, pathological uptake was detected in
the tumours, but no mediastinal involvement was detected.
The operations performed were a pneumonectomy (due to
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3
Table 2: Diagnostic characteristics of the lesions.
TNM
Stage
Cellular components
of end diagnosis
Resection
Followup
time (m)
Prognosis
1
T3N0M0
IIB
Squamous
Chondrosarcoma
Right Lo (...truncated)