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                <title><![CDATA[Clinical profile, surgical management and
outcome of bronchial carcinoids - a single centre experience]]></title>

                                    <author><![CDATA[Farooq Ahmad Ganie]]></author>
                                    <author><![CDATA[Shahbaz Bashir Dar]]></author>
                                    <author><![CDATA[Masarat-ul Gani]]></author>
                                    <author><![CDATA[Hakeem Zubair Ashraf]]></author>
                                    <author><![CDATA[Ghulam Nabi Lone]]></author>
                                    <author><![CDATA[Mudasir Hamid Bhat]]></author>
                                    <author><![CDATA[Iqra Nazir Naqash]]></author>
                
                <link data-url="https://imcjms.com/registration/journal_full_text/455">
    https://imcjms.com/registration/journal_full_text/455
</link>
                <pubDate>Wed, 15 Mar 2023 13:04:20 +0000</pubDate>
                <category><![CDATA[Original Article]]></category>
                <comments><![CDATA[IMC J Med Sci. 2023; 17(2):003]]></comments>
                <description>Abstract 
Background
and objectives: Bronchial carcinoid tumors are neuroendocrine neoplasms that
range from low-grade typical carcinoids to more aggressive atypical carcinoids
and, therefore demonstrate a wide spectrum of clinical behaviors, histologic
features and outcome. The aim of the present study was to investigate the
clinical profile, surgical management and outcome of bronchial carcinoids at a
single centre over two years period.
Materials and methods: Patients with a final histologic diagnosis of bronchial carcinoid
tumor were included in the study. Evaluation comprised of clinical history and
physical examination, postero-anterior and lateral chest radiographs, and
computed tomographic (CT) scans of the chest and upper abdomen (including liver
and adrenal glands). Performance status was assessed by the Karnofsky scale.
Pulmonary function tests were performed routinely.
Results: A total of 18
patients were included in the study. Out of 18 cases, 10 (55.6%) were female
and 8 (44.4%) were males. Sixteen (88.9%) patients had typical carcinoid tumor
and 2 (11.1%) had atypical carcinoid tumor. The tumor was located in the right
lung in 11 (61.1%) and in the left lung in 7 patients (38.9%). Surgeries
included 15 standard lobectomies and 3 bronchial sleeve resection. At one month
post surgery, there was 13-22% increase in post operative FEV1 in patients who
underwent bronchial sleeve resection while in patients who underwent lobectomy,
the post operative FEV1 was 84% of pre-operative FEV1. Post surgery, all
patients were in group A as per Karnofsky performance status.
Conclusion: Standard care of
bronchial carcinoid tumors is surgical resection, and the surgical approach
should depend on tumor’s size, location and histology.
IMC J Med Sci. 2023; 17(2):003. DOI: https://doi.org/10.55010/imcjms.17.013
*Correspondence: Farooq Ahmad Ganie, Department of Cardiovascular and Thoracic
Surgery, SKIMS, Soura, Srinagar, Kashmir, India. Email: farooq.ganie@ymail.com
&amp;nbsp;
Introduction
Bronchial carcinoid tumors are neuroendocrine
neoplasms that range from low-grade typical carcinoids to more aggressive
atypical carcinoids and therefore demonstrate a wide spectrum of clinical
behaviors and histologic features [1]. Typical and atypical bronchial
carcinoids have similar imaging features. Because most bronchial carcinoids are
located in central airways, radiologic findings are usually related to
bronchial obstruction. Central bronchial carcinoids manifest as an
endobronchial nodule, hilar or perihilar mass with a close anatomic
relationship to the bronchus [1]. The mass is usually a well-defined, round or
ovoid lesion and may be slightly lobulated at radiography and computed
tomography (CT). Associated atelectasis, air trapping, obstructing pneumonitis,
and mucoid impaction may also be seen. Peripheral bronchial carcinoids appear
as solitary nodules. Calcification is common and is easily visualized at CT.
Bronchial carcinoids demonstrate high signal intensity on T2-weighted and
short-inversion-time inversion recovery magnetic resonance images. Prognosis of
bronchial carcinoids is highly dependent on histologic findings. Typical
bronchial carcinoids generally have an excellent prognosis, whereas atypical bronchial
carcinoids have a worse prognosis. Therefore, understanding the histologic,
clinical, and radiologic features of bronchial carcinoids facilitates accurate
diagnosis and helps optimize surgical planning [2].
Standard care of bronchial carcinoid tumors is
surgical resection. Surgical approach depends on tumor’s size, location and
histology. Pneumonectomy, while effective at removing lung tumors, can carry
high morbidity and mortality by removing an entire half of a person&#039;s lung
volume. Pulmonary resection techniques are varied and categorized by the extent
of lung resected.&amp;nbsp;Bronchial sleeve resection with complete pulmonary
preservation (BSRCPP) is a classic surgical method for the treatment of benign
or low-grade bronchial tumors [3]. For elderly patients and patients with poor
cardiopulmonary function, BSRCPP is particularly advantageous because some of
these patients may not tolerate lobectomy or pneumonectomy. The use of
bronchial and arterial sleeve resections for the treatment of centrally-located
lung cancers, when available, has become the option of choice in comparison
with pneumonectomy (PN) or lobectomy. The present study evaluated the clinical
profile, surgical management and outcome of bronchial carcinoids at a single
center over two years period. 
&amp;nbsp;
Materials and methods
The study was conducted in the Department of
Cardiovascular and Thoracic Surgery, SKIMS Srinagar Kashmir from January 2020-January
2022. After local ethical clearance, patients with a final histologic diagnosis
of bronchial carcinoid tumor were assessed for surgery and enrolled in the
study. Evaluation comprised history and physical examination, posteroanterior
and lateral chest radiographs, and computed tomographic (CT) scans of the chest
and upper abdomen (including liver and adrenal glands). Pulmonary function
tests were performed routinely. All patients had a preoperative examination
with a fiberoptic bronchoscope, and in all cases endoscopic biopsy was
performed. At surgery, all specimens resected, including hilar and mediastinal
lymph nodes were sent for histologic examination. Tumors were classified
according to the current WHO/IASLC criteria for neuroendocrine tumors. Typical
carcinoids were defined as tumors greater than 5 mm in diameter, with carcinoid
morphology and less than 2 mitoses per 2 mm2, and lacking necrosis.
Tumors with a mitosis rate of 2-10 per 2 mm2, with focal necrosis or
limited necrosis, were classified as atypical carcinoid tumors [4]. All
patients underwent complete blood count, fasting blood sugar, kidney and liver
function tests. Performance status of the patients was assessed by the
Karnofsky Performance scale (KPS) [5]. KPS describes
a patient’s functional status as a comprehensive 11-point scale correlating to
percentage values ranging from 100% (no evidence of disease, no symptoms) to 0%
(death) and classified patients into following three groups: 
A: Able to carry
on normal activity and to work. No special care is needed.
B: Unable to
work. Able to stay at home and take care of most personal needs. A varying
degree of assistance is needed.
C: Unable to care
for self. Requires equivalent of institutional or hospital care. Disease may be
progressing rapidly.
&amp;nbsp;
Results
The study group comprised of 18 patients, with
10 (55.6%) female and 8 (44.4%) male patients. Age at presentation ranged from
12 to 55 years (mean: 42 years). Out of 18 cases, 16 (88.9%) patients had
typical carcinoid tumor and 2 (11.1%) had atypical carcinoid tumor. Both
patients with atypical carcinoid were aged more than 45 years. Symptoms were
present in 16 patients: cough (n= 15), fever (n=12), wheezing (n=9), hemoptysis
(n=7) dyspnea (n=7) and recurrent pulmonary infections (n=5). Two patients were
asymptomatic and bronchial carcinoid tumor was incidentally detected during
post Covid-19 illness checkup. General profile and presenting clinical features
of the study population are shown in Table-1. 
&amp;nbsp;
Table-1: General profile and presenting clinical features
of the study population (n=18) 
&amp;nbsp;
&amp;nbsp;
Location and types of the tumors: The tumor was
located in the right lung in 11 patients (61.1%) and in the left lung in 7
patients (38.9%). Features of typical carcinoid lung tumor included: tumor size
&amp;gt; 5 mm in diameter, with carcinoid morphology and less than 2 mitoses per 2
mm2. Atypical carcinoid tumor had a mitosis rate of 2 to 10 per 2 mm2,
with focal necrosis or limited necrosis.
Surgery and postoperative course: Surgeries
included 15 standard lobectomies (5 right inferior, 3 right superior, 2 right
middle, 3 left superior and 2 left inferior) and 3 bronchial sleeve resection (
2 left and 1 right). The patients who underwent lobectomy were discharged 9 to
14 days after surgery (mean duration: 12 days) and the patients who underwent
bronchial sleeve resection were discharged 7 to 11 days after surgery (mean
duration: 9 days). There was a complete resolution of symptoms immediately in
all patients, however, 2 out of 15 patients who underwent lobectomy felt
dyspnea on exertion at 15 day follow up which gradually improved. At one month,
there was 13-22 % increase in post operative FEV1 in patients who underwent
bronchial sleeve resection. In patients who underwent lobectomy, the post
operative FEV1 was 84% of pre-operative FEV1 at one month. Post surgery, all patients
were in group A (able to carry on normal activity and to work, no special care
is needed) as per Karnofsky performance status.
&amp;nbsp;
Discussion
Carcinoid tumors are a unique type of
malignant pulmonary disease. They are rare, comprising less than 2% of all
primary pulmonary neoplasms [6]. The prevalence of bronchial carcinoid tumors
is slightly higher in females [7]. The mean age of our patients at presentation
was 42 years (range 12 to 55 years), which is in line with literature. Patients
having atypical carcinoid tumors were significantly older at presentation than
patients with typical carcinoid tumors, as mentioned in various studies [8].
Bronchoscopy plays a big role in the diagnosis
of carcinoids. In majority of our cases the tumors were centrally located and
visible at endoscopic evaluation, as described by others [9]. Some authors
found bleeding to occur in two thirds of their patients and some advised
against biopsy when carcinoid was suspected. However, others disagreed,
maintaining that bronchoscopic biopsy significantly increases the diagnostic
yield without adding morbidity. In our experience, no troublesome bleeding was
reported after endoscopic biopsy.&amp;nbsp;
Preoperative radiologic evaluation and
histologic typing are mandatory in selecting the extent of surgical resection.
Newer modalities of investigation for staging bronchial carcinoid tumors that
have recently been introduced include positron emission tomography and
octreotide scintigraphy. Positron emission tomographic imaging of bronchial
carcinoid tumors demonstrates lower uptake than non–small cell lung cancers,
suggesting that the process is benign and that staging of regional lymph nodes
might be unreliable [10]. Scintigraphy with 111In-octreotide has
demonstrated reliable uptake in primary tumors and the ability to detect early
recurrences and metastases even in asymptomatic patients, suggesting that it
would be a useful tool for routine staging in the future [11]. At present,
however, decisions regarding appropriate therapy for patients with bronchial
carcinoid tumors are made on the basis of histologic features and clinical
staging of the tumor by bronchoscopy and CT scan.
The success of current surgical management of
bronchial carcinoids is influenced by the recurrence rates and survival
patterns. In patients with centrally located typical carcinoid tumor of the
lung, we think that bronchial sleeve resection or sleeve lobectomy should be
considered, when possible, because local recurrence is rare and survival is
excellent. Despite the low local recurrence rate, early-stage typical
carcinoids should be considered as low-malignancy neoplasms and should be
managed by an anatomic resection to secure the least risk of recurrence. On the
other hand, local recurrence rate and long-term survival are both unfavorably
affected by the finding of atypical subtype. If this histologic subtype is
identified, a more extensive surgical approach such as lobectomy or
pneumonectomy associated with lymph node dissection is mandatory.
Standard care of bronchial carcinoid tumors is
surgical resection, with the surgical approach depending on tumor’s size,
location and histology. Pneumonectomy, while effective at removing lung tumors,
can carry high morbidity and mortality by removing an entire half of a person&#039;s
lung volume. Pulmonary resection techniques are varied and categorized by the
extent of lung resected.&amp;nbsp;Bronchial sleeve resection with complete
pulmonary preservation (BSRCPP) is a classic surgical method for the treatment
of benign or low-grade bronchial tumors.
&amp;nbsp;
Funding: This research
received no internal or external funding.
&amp;nbsp;
Conflicts of
interest: The authors declare no conflict of
interest.
&amp;nbsp;
References
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&amp;nbsp;
&amp;nbsp;
&amp;nbsp;
Cite
this article as:
Ganie FA, Dar SB, Gani M, Ashraf HZ, Lone GN,
Bhat MH, Naqash IN. Clinical profile, surgical management and outcome of
bronchial carcinoids - a single centre experience. IMC J Med Sci. 2023; 17(2): 003. DOI: https://doi.org/10.55010/imcjms.17.013
&amp;nbsp;</description>

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