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Journal of Clinical Chemistry and Laboratory Medicine

Journal of Clinical Chemistry and Laboratory Medicine
Open Access

ISSN: 2736-6588

Case Report - (2023)Volume 6, Issue 2

Neuroendocrine Lung Tumor and Metastatic Intrapulmonary Lymph Nodes

Habib Mantilla Gaviria1* and Willfredy Castano Ruiz2
 
*Correspondence: Habib Mantilla Gaviria, Department of General Surgeon, University of El Bosque, Bogota, Colombia, Email:

Author info »

Abstract

Background: Multifocal neuroendocrine tumors of the lung are rare, usually having low nodal involvement in early stages. We bring to the literature a case of a typical multifocal carcinoid associated to tumors with Intra-Pulmonary Lymph Node (IPLN) involvement.

Case presentation: 59-year-old female asymptomatic patient with multiple nodules in the right lower lobe, PET-CT with hypermetabolic nodule, adequate pulmonary function, for which a right lower lobectomy was performed plus intrapulmonary lymph nodes dissection in the fresh surgical specimen. The lymph nodes of stations 11, 12, 13 and 14 were sent to pathology. The pathology laboratory report showed that stations 10, 11, 12 and 13 were negative, but station 14 was positive. Thus, changing the stage from Ia2 to IIb.

Conclusion: This patient had an upstaging because of IPLN were positive for metastasis. The search for a more accurate oncologic staging through intrapulmonary lymph node may allow a more accurate staging and therefore a better treatment for the patient regardless type histology.

Keywords

Pulmonary neuroendocrine tumor; Intrapulmonary lymph nodes; Lymphadenectomy; Pathology

Introduction

Neuroendocrine Tumors (NETs) of the lung have an incidence of 0.35 to 1.62 per 100,000 inhabitants. The most frequent age is between 48 and 70 years, and there is no relationship with smoking [1].

NETs can be Typical Carcinoids (TC), Atypical Carcinoids (AC) and neuroendocrine carcinomas such as small and large cell carcinomas. Nodal metastases occur up to 17% in N1 stations in TC and 37.5% in AC. This defines the risk of locoregional recurrence and Overall Survival (OS). Current reports do not specify the N1 stations involved, especially 12, 13 and 14 [2]. Current general practice does not include routine IPLN screening in pathology laboratories, creating a group of patients with understaging if only stations 12, 13, or 14 are positive.

We present the first case in the literature of multifocal NET with IPLN dissection in search of metastatic lymph nodes, which determined N1 positive and under staging if they had not been explored. This makes it possible to group patients into more precise stages and therefore offer them more appropriate treatment.

Case Presentation

A 59-year-old female asymptomatic patient with a history of arterial hypertension, grade I obesity, prediabetes with HbA1c of 6.1% and thrombocytopenic purpura. During controls with hepatology, a thoracic Computed Tomography (CT) scan was performed and 3 pulmonary nodules were found in the Right Lower Lobe (RLL) showed in Figure 1. One of 13 mm with central position and others of 9 and 6 mm peripherals, without mediastinal adenopathy’s. PET-CT hypermetabolic lesion with SUV: 3.88 corresponding to the 13 mm nodule as shown in Figure 2. Spirometry with FEV1 126% and DLCO 124%. The patient is considered a candidate for right lower lobectomy by Video-Assisted Thoracoscopic Surgery (VATS) (Figures 1 and 2).

pulmonary

Figure 1: Chest CT: 13mm pulmonary nodule (green arrow).

nodule

Figure 2: PET-CT: 13mm pulmonary nodule with SUV 3.88 (white arrowhead).

VATS wedge resection single-port technique of the 9 mm nodule was performed and sent to freezing, reporting a typical carcinoid tumor. Considering that the hypermetabolic lesion is central and the high probability of malignancy, the right lower lobectomy is completed with mediastinal lymph node dissection and intrapulmonary node dissection (stations 12, 13 and 14) on the fresh specimen, immediately after completing the procedure.

Intrapulmonary lymph node dissection technique: Starting from the lobar bronchus distally, following the peri bronchial route and obtaining the lymph nodes of stations 12, 13 and 14. Which are then sent to pathology duly labeled?

Pathology report

Typical multifocal neuroendocrine tumors without lymphovascular or perineural invasion of 9mm in upper segment (sample sent to freezing), another one of 14 mm and a tumor of 4 mm. 29 mediastinal nodes without tumor involvement and 1 of 6 nodes involved by tumor (metastasis of 2mm) in N1, being the nodal station 14R.

Analyzed in the chest staff, concluding a stage IIB (T1bN1M0 multifocal) with complete lobar resection and follow-up is defined.

The patient gives informed consent for publication of her case.

Results and Dicsussion

Nodal involvement of NET is infrequent. Our case has a multifocal NET and IPLN (station 14) metastatic component. There is no report in the literature of this type of presentation in multifocal NET. Most of the studies include only adenocarcinomas or squamous cell carcinoma, for this reason we consider it important to contribute our case to the current literature [3].

It has been described that pathology reports do not inform intrapulmonary nodal status up to 90%, this may leave a gap in oncologic staging, which is why it is important to investigate the behavior of IPLN [4].

Dr. Osarogiagbon describes the IPLN dissection with the lung lobe in formaldehyde and following the peribronchial pathway. In our case we decided to perform the dissection in the RLL in the operating room once the specimen has been extracted, considering that the histopathological evaluation of these lymph nodes is not routinely performed in pathology laboratories in our country [5].

Different authors have demonstrated upstaging when analyzing IPLN histology. Lei, et al. published a study with 234 patients, identifying lymph node metastases in stations 12, 13 and 14 between 6.8% and 12% [6]. If we had not dissected the IPLN, the patient's staging would be lower. Pathipati, et al. published a study with 98 patients with 16.6% of metastases in N1 and showed a higher percentage of recurrence (29% vs. 6%; p: 0.01%) associated with lymph node metastases, being higher in NER/CT (11/NER, 8/CT and 3/CA) [7].

These studies do not specify which stations were positive, conducted a study with 435 patients (170 study group in which stations 10-14 were routinely examined vs. 265 in the control group in which only stations 10-12 were examined), found that the study group had better OS and DFS (5-year OS rate, 89 ± 3% vs. 77 ± 4%, P=0.027; 5-year DFS rate, 81 ± 4% vs. 67 ± 4%, P=0.021), in its multivariate analysis, the collection of IPLN 13 and 14 had a significant impact on OS (Hazard Ratio (HR), 0.518; 95% Confidence Interval (CI), 0.298-0.898) and DFS (HR, 0.590; 95% CI, 0.387-0.901).

Conclusion

This is just one case report on the metastatic involvement of IPLN in a multifocal NET and it is interesting to perform the dissection of stations 12, 13 and 14 because they have shown an important role in staging and OS. This is a reminder to readers about the presence of IPLNs and that their metastatic involvement may be present. Due to de lack of information in NET and IPLN we have to explore more this area.

Ethics Approval

This document has been approved by the Pablo Tobon Uribe Hospital’s Medical Ethics Committee and the personal data of the patient are protected for this reason they are not disclosed in the article.

Consent for Publication

The patient gave his consent for the publication of his case.

Author's Contributions

All the authors took part in the patient’s hospitalization and in writing the article.

Acknowledgment

We thank the patient for allowing us to contribute her case to the medical literature.

References

Author Info

Habib Mantilla Gaviria1* and Willfredy Castano Ruiz2
 
1Department of General Surgeon, University of El Bosque, Bogota, Colombia
2Department of Thoracic Surgeon, Pablo Tobon Uribe Hospital, Medellin, Colombia
 

Citation: Gaviria HM, Ruiz WC (2023) Neuroendocrine Lung Tumor and Metastatic Intrapulmonary Lymph Nodes. J Clin Chem Lab Med. 6:269.

Received: 02-Jun-2023, Manuscript No. JCCLM-23-24742; Editor assigned: 05-Jun-2023, Pre QC No. JCCLM-23-24742 (PQ); Reviewed: 19-Jun-2023, QC No. JCCLM-23-24742; Revised: 26-Jun-2023, Manuscript No. JCCLM-23-24742 (R); Published: 03-Jul-2023 , DOI: 10.35248/JCCLM.23.6.269

Copyright: © 2023 Gaviria HM, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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