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Maltoma of Lung in a Glass BlowerMahadev Patil, MBBS Senior resident, Department of Respiratory Medicine, T.N. Medical College & B.Y.L. Nair Charitable Hospital AND J.M. Joshi, M.D. Professor and Head, Department of Respiratory Medicine T.N. Medical College & B.Y.L. Nair Charitable Hospital A 65-year-old man was referred to our chest clinic for preoperative assessment before undergoing repair of a fractured neck of his femur. His chest radiograph was abnormal (figure 1).
He complained of cough with minimal mucopurulent expectoration
and fever, which had not responded to a ten-day course of
gatifloxacin, 400 mg daily.He was a non-smoker and had no
significant medical or surgical illness in the past. He had worked
as a glass blower (mouth blower) for 40 years and had retired from
work 5 years before this assessment. The glass blowing was done in
a workshop with a glass pipe made of borosilicate (figure 2). This
pipe was used to blow the molten glass to give the desired shape to
make scientific glass equipment like test tubes and flasks. The
glass tube to be blown was loaded on the borosilicate glass pipe.
The glass is then melted by holding it over an arc light generated
by flaming a mixture of air with liquefied petroleum gas (figure
3). The molten glass is then blown by mouth to give the desired
shape (figures 4 and 5).
Figure 3: Arc light used to melt glass. (Photographs taken at a workshop in Mumbai, India, with informed consent of a glass blower at work)
On physical examination, tubular bronchial breath sounds and crackles were heard in the right lower interscapular and infrascapular region. His hemoglobin was 12.8 g/dL; his leukocyte count was 12,400 / mm3 with a differential count of neutrophils 70% and lymphocytes 30%. Sputum smear and culture was negative for bacteria, acid-fast bacilli and fungi. Arterial blood gases on room air showed a pH of 7.39, PaO2 of 78 mm Hg, PaCO2 of 44 mm Hg, and HCO3 26 mmols/L. A computerized tomography (CT) scan ofthethorax (figure 6) showed consolidation in the right lower lobe. There was no hilar or mediastinal lymphadenopathy or narrowing of the right lower lobe bronchus.
Another chest radiograph and CT, after completing the course of antibiotics, showed no change in the consolidation. The patient underwent a CT-guided fine needle aspiration biopsy, which showed a low-grade lymphoproliferative disorder. Immunohistochemistry showed CD20-positive, CD43-positive, CD5-negative, CD10-negative, and Bcl 2-negative antigen markers. He refused surgery and was treated with cyclophosphamide, vincristine, and prednisolone. After 3 cycles of chemotherapy the patient developed an acute myocardial infarction, which was treated successfully. Further chemotherapy was not given. His chest radiograph showed clearing of the lung lesion (figure 7). Presently he is well with no recurrence and takes only low dose aspirin and isosorbide dinitrate for his ischemic heart disease.
Question 1Given the history, clinical findings, chest radiograph, and CT scan images, which one of the following is the LEAST likely diagnosis?
AnswerThe correct answer is b. The chest radiograph and CT scan show an opacity with air bronchogram indicating a consolidation or pneumonia picture. Only silicosis of the listed causes does not generally cause lower lobe consolidation. The chest radiograph showed no evidence of resolution after an adequate course of antibiotics characterizing this as a non-resolving pneumonia. Causes for non-resolving pneumonia include:
The immunohistochemical findings in this case were consistent with extranodal, marginal zone B-cell lymphoma of mucosa associated lymphoid tissue (MALT) of the lung. The immunohistochemistry showed the B cell phenotype (CD19, CD20 positive) and excluded centrifollicular non-Hodgkins lymphoma (NHL)-B, mantel NHL-B and chronic lymphocytic leukaemia-type lymphoma by showing the lack of CD5 and CD10 surface antigens [1]. Primary malignant non-Hodgkin’s lymphomas arising in MALT develop most frequently in the stomach, but also in the bowel, salivary glands, larynx, thyroid gland, and lung [1,2,3]. Accordingly, when located in the lung, this lymphoma appears to arise from bronchus-associated lymphoid tissue (BALT) [3]. The Revised European American Lymphoma classification and the World Health Organization in 1994 incorporated mucosa-associated lymphoma as a distinct subgroup of non-Hodgkin lymphoma under the term extranodal, marginal zone lymphoma of MALT. Primary pulmonary lymphoma is defined as a clonal lymphoid proliferation affecting the lungs or bronchi in a patient with no detectable extrapulmonary involvement at diagnosis or in the subsequent 3 months. Primary pulmonary lymphomas are rare tumors comprising about 3% of all extranodal lymphomas, and only 0.5% of all pulmonary malignancies. Question 2Which one of the following manifestations is LEAST likely to be seen in glass blowers?
AnswerThe correct answer is e. Pleural involvement is rare in glass blowers, although it may be involved secondary to malignancies at other sites. An increased risk of lung, stomach, colon, and bladder cancer has been reported in previous studies among glass workers. Metallic compounds and other agents used in the manufacture of glass are likely to be responsible for the cancer risks observed in glassworkers. Four cohort studies of workers involved in glass manufacture - one at a plant in Italy among art glass workers, [4] two at glass factories in Finland [5] and one in Sweden among art glass-workers [6] found increased risks for lung cancer. Another population-based case-control study in China found a significantly increased risk for lung cancer in female glass-workers and a nonsignificantly decreased risk in male glass, ceramics and enameled product workers [7]. The epidemiological evidence for aetiologies of MALT lymphomas, a subset of NHL, is limited. The stomach is the most frequent site of MALT lymphoma. During chronic antigenic stimulation (by Helicobacter pylori, for example), MALT can develop in the stomach and undergo secondary lymphomatous transformation arising from marginal zone B-cells. In order to develop, the malignant B-cell clone requires the presence of T-cells specifically directed against H. pylori antigens. No triggering antigens have so far been identified in the lung, but chronic antigenic stimulation in certain autoimmune disorders (systemic lupus erythematosus, multiple sclerosis, Hashimoto's thyroiditis and particularly Gougerot-Sjögren's syndrome) is considered to affect the onset of pulmonary MALT lymphoma. [8] It is interesting to consider the current epidemiological evidence of occupational factors in NHL. A number of occupations that involve exposures to electromagnetic fields, treated and fresh wood, metals, and solvents have been found to be associated with an increased risk of developing NHL. [9] A Canadian study found an increased risk of NHL among males exposed to benzidine, mineral, cutting, or lubricating oil, pesticides, and herbicides and females exposed to pesticides and wood dust. [10] The findings of this study suggest that occupational exposure to specific chemicals plays an important role in the development of NHL. Since the risk of NHL is elevated in persons with acquired and congenital immune deficiency as well as autoimmune disorders, chemicals such as polychlorinated biphenyl compounds (PCBs), chlordanes, dioxins, chlorophenols and organic solvents all of which have been associated with increased risk for NHL may do so because of their immunotoxic effects. [11] Traditional non mechanized techniques such as glass blowing are used in the manufacture of crystal and art glass and can result in exposure to lead, arsenic and antimony oxides. Other potential exposures in glass manufacture include silica, asbestos, other metal oxides and polycyclic aromatic hydrocarbons. [12] The evidence that favors a causal association between exposures in the glass manufacturing industry and cancer is: a reasonably consistent association with lung cancer; a larger lung cancer risk than can reasonably be explained by non-occupational confounding factors; the presence of human lung carcinogens in some components of the glass manufacturing industry. [12] Question 3Which ONE of the following is NOT a characteristic CT scan appearance of MALTOMA of the lung?
AnswerThe correct answer is e. The common radiographic appearances are pulmonary masses or mass-like areas of consolidation or nodules, unilateral or bilateral, and in peribronchial or bronchovascular distribution. Frequently, air bronchograms are seen within the nodules and masses. The patent airways within the consolidated lung appear dilated and, occasionally, can be mistaken for cavitation. Lymphadenopathy may also be observed on CT imaging. High-resolution CT scans may show areas of ground-glass opacity and peribronchovascular thickening at the tumor margins. [2,3,13] In the 11 patients reviewed by Kinsley et al, [14] the most common CT appearance of pulmonary mucosa-associated lymphoid tissue lymphoma was consolidation with air bronchograms, correlating histologically with a cellular lymphocytic infiltrate expanding the interstitium and compressing adjacent alveoli, producing air bronchograms. Question 4Which of the following is the usual treatment for this disease?
AnswerThe best answer is e. In the absence of any prospective studies, the optimal therapy
remains unclear. In most series, surgical resection, either alone
or in combination with chemotherapy, has been the mainstay of
therapy. Chemotherapy has also been used in patients with residual
disease after resection or in those with extrapulmonary
involvement. No difference in response rates was seen with
single-agent chemotherapy or in multiple chemotherapeutic drug
regimes. The prognosis is excellent for patients with localized
MALT lymphomas. Most series have reported a 5-year survival rate of
greater than 80% and a median survival time of 10 years. [13] Local
and extrathoracic relapse have been noted, making long-term
surveillance necessary. Although transformation to high-grade
lymphoma has been reported, these cases may represent large B-cell
lymphomas that have been initially mistaken for MALT
lymphomas.
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