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Sanjay Gandhi institute of trauma and orthopedics,
Bengaluru.
On Aug 2018




Dr. Mamta Gupta,
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Consultant
(Ex HOD Obs &Gynae, Hindu Rao Hospital and associated NDMC Medical College, Delhi)
Aug 2018




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Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
E-mail: drrajendrak1@rediffmail.com
On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
Strengths of the journal: The journal has an online first facility in which the accepted manuscripts may be published on the website before being included in a regular issue of the journal. This cuts down the time between their acceptance and the publication. The journal is indexed in many databases, though not in PubMed. The editorial board should now take steps to index the journal in PubMed. The journal has a system of notifying readers through e-mail when a new issue is released. Also, the articles are available in both the HTML and the PDF formats. I especially like the new and colorful page format of the journal. Also, the access statistics of the articles are available. The prepublication and the manuscript tracking system are also helpful for the authors.
Areas for improvement: In certain cases, I felt that the peer review process of the manuscripts was not up to international standards and that it should be strengthened. Also, the number of manuscripts in an issue is high and it may be difficult for readers to go through all of them. The journal can consider tightening of the peer review process and increasing the quality standards for the acceptance of the manuscripts. I faced occasional problems with the online manuscript submission (Pre-publishing) system, which have to be addressed.
Overall, the publishing process with JCDR has been smooth, quick and relatively hassle free and I can recommend other authors to consider the journal as an outlet for their work."



Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
E-mail: ravi.dr.shankar@gmail.com
On April 2011
Anuradha

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.


Dr. Anuradha
E-mail: anuradha2nittur@gmail.com
On Jan 2020

Important Notice

Case report
Year : 2023 | Month : January | Volume : 17 | Issue : 1 | Page : OD06 - OD08 Full Version

Bronchioloalveolar Carcinoma Mimicking as Pneumonia: A Case Report


Published: January 1, 2023 | DOI: https://doi.org/10.7860/JCDR/2023/60149.17267
Bhavesh Patel, Cheguri Vasavi, Arti Dhawal Shah, Chirag Chakravarti, Anchal Jain

1. Associate Professor, Department of Respiratory Medicine, Smt. B.K. Shah Medical Institute and Research Centre, Vadodara, Gujarat, India. 2. Resident, Department of Respiratory Medicine, Smt. B.K. Shah Medical Institute and Research Centre, Vadodara, Gujarat, India. 3. Head, Department of Respiratory Medicine, Smt. B.K. Shah Medical Institute and Research Centre, Vadodara, Gujarat, India. 4. Assistant Professor, Department of Respiratory Medicine, Smt. B.K. Shah Medical Institute and Research Centre, Vadodara, Gujarat, India. 5. Senior Resident, Department of Respiratory Medicine, Smt. B.K. Shah Medical Institute and Research Centre, Vadodara, Gujarat, India.

Correspondence Address :
Dr. Cheguri Vasavi,
Resident, Department of Respiratory Medicine, Smt. B.K. Shah Medical Institute and Research Centre, Vadodara, Gujarat, India.
E-mail: vasavicheguri011@gmail.com

Abstract

Bronchioloalveolar Carcinoma (BAC) also known as alveolar cell carcinoma is a subtype of adenocarcinoma that is more common in women and non smokers. It accounts for almost 5% of all lung cancers. Bronchioloalveolar carcinoma may appear as a wide variety ranging from solitary nodule to patchy, lobar or multilobar opacities. The mucinous, non mucinous, ambiguous or mixed are the histological types of BAC. The mucinous variety of BAC sometimes may present as a consolidation which is indistinguishable from an infective pneumonia on a radiological picture. Hereby, authors present a case of 65-year-old male patient, who was evaluated for non resolving pneumonia for a time span of one year. He presented to the Respiratory Medicine Outpatient Department with a cough and expectoration for the past nine months. Antibiotic courses did not provide the patient any sort of relief and there was no change in the size of the lesion. Chest X-ray has shown right sided non homogenous opacity and later Contrast Enhanced Computerised Tomography (CECT) thorax and biopsy (Computed Tomography-guided {CT-guided}) was done from the same site for further evaluation. Cytology done from CT-guided biopsy sample showed typical lepidic growth pattern. Histopathologically, it showed mucinous variety of BAC. Usually, the patients have no symptoms, but an abnormal chest X-ray, while a few have features like coughing with expectoration and pain in the chest. Only cytology or biopsy can help with a proper diagnosis, which can be done via needle biopsy (CT or fluoroscopy-guided) or transbronchial biopsy and Bronchioloalveolar Lavage (BAL). It has rarely been documented in the literature that BAC masquerades as a consolidation with very little change.

Keywords

Adenocarcinoma, Consolidation, Mucinous variety

Case Report

A 65-year-old male, an accountant by profession and a non smoker, presented to the Respiratory Medicine Outpatient Department with a cough and expectoration for the past nine months. Sputum was 4-5 cc/day, whitish, mucoid, non foul-smelling, non blood tinged. He had no history of chest pain, breathlessness, fever, chills, rigours, haemoptysis, hoarseness of voice, loss of weight, or loss of appetite. The patient had type 2 diabetes mellitus and was taking his medicine on a regular basis. He had no other major illnesses. On general examination, he was conscious, coherent and well-oriented to time, place and person. Icterus, cyanosis, clubbing, oedema, and lymphadenopathy were not present. He was afebrile, with a pulse of 96 beats per minute, a respiratory rate of 20, a blood pressure of 122/80 mmHg, and a SpO2 of 98% on room air. Breath sounds were reduced throughout the right interscapular area during a respiratory system assessment.

Routine microbiological investigations were within normal limits. Sputum for Acid Fast Bacilli (AFB) was mucoid negative. Chest X-ray showed right-sided non homogenous opacity (Table/Fig 1) and later Contrast Enhanced Computerised Tomography (CECT) thorax was done, which showed an ill-defined patch of consolidation with surrounding Ground Glass Opacities (GGO) with interlobular septal thickening in the anterior segment of the right upper lobe of size 6.7×4.1×5.2 cm, with postcontrast enhancement (Table/Fig 2). The provisional diagnosis at this stage was a non resolving consolidation, probably BAC and also we had the differential diagnosis of inflammatory processes like bronchiolitis obliterans or hypersensitivity pnuemonitis as the radiological features are similar and along with it, the presenting features (cough, chest pain, and sputum production) are pretty much similar to other inflammatory processes.

For further evaluation, A CT-guided biopsy was done from the anterior segment of right upper lobe. Cytology done from CT guided biopsy sample showed the cells arranged in sheets and a honeycomb-pattern with a typical lepidic pattern with cells having hyperchromatic nuclei, vacuolated to clear abundant cytoplasm suggestive of mucinous bronchioloalveolar adenocarcinoma. Histopathology report showed columnar cells containing mucin lining the respiratory spaces in lepidic fusion without invading stroma suggesting bronchioloalveolar carcinoma (Table/Fig 3). Immunohistochemistry (IHC) has shown tissue infiltration by a tumour composed of complex back-to-back glands lined by mucin-secreting columnar cells displaying mild nuclear anaplasia. Lymphovascular and perinuclear invasions are not seen. Tumour cells are diffuse and strongly positive for CK7, TTF1, and Napsin A and negative for CK20, suggesting primary well differentiated mucinous adenocarcinoma of the lung (Table/Fig 4). A cancer targeted gene panel showed a mutation to the KRAS gene. By this, the final diagnosis of the present case was Bronchioloalveolar Carcinoma (BAC).

To identify the metastasis of the tumour, Positron Emission Tomography and Computed Tomography (PET-CT) scan was done (Table/Fig 5), which revealed an area of consolidation and interlobular septal thickening with enhancement and mild Flourodeoxy Glucose (FDG) activity in the anterior segment of the RUL-likely primary. FDG avid GGO in bilateral lungs predominantly peripheral.

A repeat CT scan was done after three months period. As compared to the previous CT scan, patchy areas of consolidation in the right upper lobe, right middle lobe, and superior segment of the right lower lobe of the lung had newly appeared (Table/Fig 6). The patient is now undergoing combined treatment chemotherapy with cisplatin (90 mg) and premetrexed (800 mg) in cycles and radiotherapy.

Discussion

The BAC can be defined as neoplasm which is not of central origin, but is peripherally located; therefore the term “bronchiolo” but not “bronchioloalveolar” carcinoma. It grows along alveolar septa and the lung parenchyma remains intact. BAC, as described earlier, is divided into non mucinous, mucinous, and mixed subtypes, with the non mucinous variety being more common, consisting of hobnail (cuboidal) cells with apical nuclei, while the present case is mucinous type of BAC, consisting of tall columnar cells with abundant pale cytoplasm with basal nuclei resembling goblet cells (1). These tumours are a diverse group of peripheral lung tumours, that can develop from any epithelial cell within or distal to terminal bronchioles (2). The pattern of growth is lepidic, meaning the proliferation of tumour cells lining the alveolar walls occurs in a 7uniform manner, using them as a scaffold with no stromal or vascular invasion. BAC is now being termed as adenocarcinoma in-situ (3). It differs clinically from other types of non small cell lung cancer in certain features. These include a female predominance, particularly in East Asians; no or little smoking history; a slow course. In the present case report, patient is an old aged male, non smoker, presented with the complaints of cough with expectoration, since nine months with no other symptoms. Cough, chest pain, breathlessness, loss of appetite, loss of weight, haemoptysis being the most common presenting symptoms, very rarely patients can present with sudden haemoptysis requiring intubation (4). Bronchorrhoea is unusual and a late manifestation seen only with diffuses BAC (5). Very rarely BAC may present as recurrent pneumonias associated with asymptomatic peripheral eosinophilia (6).

If a patient who ordinarily has pneumonia does not have a fever, leucocytosis, or responds to medications, the physician should be suspicious about BAC (7). In the current case, the patient showed a consolidation with surrounding GGO with interlobular septal thickening in the right upper lobe, which led to the suspicion of pneumonia mimicking malignancies. BAC has distinct chest computed tomographic findings, sometimes small, peripheral nodules and, less frequently, as pneumonic-type consolidation or diffuse, inoperable lesions. Solid or partly solid attenuation, the presence of air-containing gaps, and the lack of contractive changes are other radiographic markers of localised mucinous BACs (8). Bronchoscopic examination is normal, but sometimes presents as a neoplastic mass within the lumen if a tumour is present centrally, brochial stenosis or compression from outside due to lymph node metastasis. Sometimes, the patients undergo an inconclusive bronchoscopy and receive several courses of antibiotics including anti-tubercular therapy without relief (9).

After confirmation of diagnosis, patient was started on chemotherapy with cisplatin and premetrexed along with radiotherapy with 60 Gy (2Gy/fraction) in cycles. Prognosis depends on size of scar, size of invasive component and pattern of invasion as the patients with small, peripheral BAC have very good prognosis (10). BAC patients have a considerably higher one year survival rate, than those with other histological subtypes of Non Small Cell Lung Cancer (NSCLC) (11). In a study by Yotsukura M et al., no reoccurrence of either of these cancers was observed in a group of 542 people after surgical removal. The estimated disease-specific survival rates were 100 percent (12). Lobectomy is the preferred treatment for pneumonic consolidation. When there is multifocal involvement, segmentectomy or wedge resection may be performed. If positive for PDL-1 receptor, immunotherapy with nivolumab or pemrolizumab can be given. Rapid responses have been observed, when specific mutations in the epidermal growth factor receptor are present (13). In the event of a recurrence, lung transplantation may be useful.

Conclusion

Bronchioloalveolar carcinoma, due to its resemblance with pneumonia the diagnosis and treatment are often delayed. In the current scenario, the patient had a presentation similar to pneumonia which was not responding to antibiotics. In order to diagnose the condition, CT-guided biopsy was done which showed mucinous type of BAC which led to the early initiation of treatment. Bronchoscopic examination might be normal in most of the cases and the use of Positron Emission Tomography (PET) is ineffective in determining the difference between inflammatory and infective aetiology. Hence, biopsy must always be considered when an pneumonia-like picture does not respond to antibiotic medication.

References

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Ingbar DH. Fishman’s pulmonary diseases and disorders Ann Am Thorac Soc. 2015;12(8):1255-56.
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Seaton A, Leitch AG, Seaton D. Crofton and Douglas’s respiratory diseases. John Wiley & Sons; 2008 Apr 30.
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Lasafin KJ. Diffuse Bronchoalveolar Carcinoma: A rare type of pulmonary adenocarcinoma. American Journal of Respiratory and Critical Care Medicine. 2018;197:A4047.
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Kambayashi T, Ono N, Noguchi T, Kamakari K, Terada Y. Bronchioloalveolar carcinoma with acute respiratory failure due to hemoptysis; report of a case. Kyobu Geka. 2004;57(12):1161-64. Japanese. PMID: 15553039.
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Barsky SH, Cameron R, Osann KE, Tomita D, Carmack Holmes E. Rising incidence of bronchioloalveolar lung carcinoma and its unique clinicopathologic features. Cancer. 1994;73(4):1163-70. 3.0.CO;2-J>[crossref] [PubMed]
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Henry DW, Rosenthal A, McCarty DJ. Adenocarcinoma of the lung associated with eosinophilia and hidebound skin. The Journal of Rheumatology. 1994;21(5):972-73.
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Thompson WH. Bronchioloalveolar carcinoma masquerading as pneumonia. Respir Care. 2004;49(11):1349-53. PMID: 15562552.
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Sawada E, Nambu A, Motosugi U, Araki T, Kato S, Sato Y, et al. Localised mucinous bronchioloalveolar carcinoma of the lung: Thin-section computed tomography and fluorodeoxyglucose positron emission tomography findings. Jpn J Radiol. 2010;28(4):251-58. Doi: 10.1007/s11604-009-0414-4. Epub 2010 May 29. PMID: 20512541. [crossref] [PubMed]
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Mir E, Sareen R, Kulshreshtha R, Shah A. Bronchioloalveolar cell carcinoma presenting as a “non resolving consolidation” for two years. Pneumonol Alergol Pol. 2015;83(3):208-11. Doi: 10.5603/PiAP.2015.0033. PMID: 26050981. [crossref] [PubMed]
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Travis WD, Garg K, Franklin WA, Wistuba II, Sabloff B, Noguchi M, et al. Bronchioloalveolar carcinoma and lung adenocarcinoma: The clinical importance and research relevance of the 2004 World Health Organization pathologic criteria. J Thorac Oncol. 2006;1(9 Suppl):S13-19. PMID: 17409995. [crossref]
11.
Read WL, Page NC, Tierney RM, Piccirillo JF, Govindan R. The epidemiology of bronchioloalveolar carcinoma over the past two decades: Analysis of the SEER database. Lung Cancer. 2004;45(2):137-42. Doi: 10.1016/j.lungcan.2004.01.019. PMID: 15246183. [crossref] [PubMed]
12.
Yotsukura M, Asamura H, Motoi N, Kashima J, Yoshida Y, Nakagawa K, et al. Long-term prognosis of patients with resected adenocarcinoma in situ and minimally invasive adenocarcinoma of the lung. J Thorac Oncol. 2021;16(8):1312- 20. Doi: 10.1016/j.jtho.2021.04.007. Epub 2021 Apr 27. PMID: 33915249. [crossref] [PubMed]
13.
Reckamp KL. Targeted therapy for patients with metastatic non small cell lung cancer. J Natl Compr Canc Netw. 2018;16(5S):601-04. Doi: 10.6004/ jnccn.2018.0046. PMID: 29784736. [crossref] [PubMed]

DOI and Others

DOI: 10.7860/JCDR/2023/60149.17267

Date of Submission: Sep 10, 2022
Date of Peer Review: Oct 28, 2022
Date of Acceptance: Nov 16, 2022
Date of Publishing: Jan 01, 2023

AUTHOR DECLARATION:
• Financial or Other Competing Interests: None
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. Yes

PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: Sep 28, 2022
• Manual Googling: Nov 04, 2022
• iThenticate Software: Nov 15, 2022 (4%)

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  • EBSCOhost
  • Google Scholar
  • HINARI Access to Research in Health Programme
  • Indian Science Abstracts (ISA)
  • Journal seek Database
  • Google
  • Popline (reproductive health literature)
  • www.omnimedicalsearch.com