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1.
Intern Med ; 59(10): 1295-1298, 2020.
Article in English | MEDLINE | ID: mdl-32418954

ABSTRACT

A 56-year-old healthy man who was a current smoker died from fulminant tracheobronchial aspergillosis despite a month of treatment with a combination of intravenous anti-fungal agents that had been started immediately after the diagnosis. This case report is important for understanding and managing fulminant Aspergillus infections in healthy subjects, although the pathogenesis and underlying pathways are still unknown.


Subject(s)
Antifungal Agents/therapeutic use , Aspergillosis/drug therapy , Bronchitis/drug therapy , Bronchitis/microbiology , Tracheitis/drug therapy , Tracheitis/microbiology , Aspergillosis/diagnosis , Fatal Outcome , Humans , Male , Middle Aged
2.
Kyobu Geka ; 71(12): 1013-1017, 2018 11.
Article in Japanese | MEDLINE | ID: mdl-30449869

ABSTRACT

Pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma is associated with pre-existing infections or autoimmune disorders. We report a case of lung cancer initially suspected of MALT lymphoma. The patient was a 73-year-old woman. Complete screening examinations identified a tumor in the right middle lobe. Transbronchial lung biopsy revealed the infiltration of CD20+/CD79a+ lymphocytes invading the structure of the alveolus. MALT lymphoma was suspected, and the middle lobe was resected. The tumor was primarily invasive mucinous carcinoma, and lymphocytic infiltration was observed around the tumor. The monoclonal expansion of B cells and genetic and chromosomal abnormalities which are criteria for the diagnosis of MALT lymphoma were not demonstrated and the lesion was diagnosed as reactive lymphoid infiltrates. Marked lymphocytic infiltration regardless of neoplastic or reactive may suggest the presence of latent lesions.


Subject(s)
Adenocarcinoma, Mucinous/pathology , Lung Neoplasms/pathology , Lung/pathology , Lymphoma, B-Cell, Marginal Zone/pathology , Aged , Biopsy , Diagnosis, Differential , Female , Humans , Lymphocytes/pathology
3.
Invest New Drugs ; 36(4): 715-717, 2018 08.
Article in English | MEDLINE | ID: mdl-29546681

ABSTRACT

Small-cell lung cancer (SCLC) combined with epidermal growth factor receptor (EGFR) mutations is extremely rare, and standard chemotherapeutic strategies have not yet been established. In the present study, we report a case of a 67-year-old man who presented with combined SCLC with EGFR mutation (exon 19 deletion). Systemic chemotherapy with cisplatin and irinotecan was initiated as first-line chemotherapy, and computed tomography findings revealed tumor shrinkage after two cycles of chemotherapy. However, after the third cycle of the treatment, disease progression was observed including the appearance of pleural and pericardial effusion. Cytologic examination of pleural and pericardial effusion revealed adenocarcinoma and no characteristics of SCLC, and an EGFR mutation was detected, in line with the initial diagnosis. Afatinib was then administered as second-line chemotherapy, which resulted in a partial response that lasted for 6 months. Re-biopsy after resistance to first-line chemotherapy suggested that the adenocarcinoma component harboring the EGFR mutation became dominant in association with disease progression, and afatinib provided clinical efficacy as second-line chemotherapy.


Subject(s)
Afatinib/therapeutic use , Lung Neoplasms/drug therapy , Mutation/genetics , Protein Kinase Inhibitors/therapeutic use , Small Cell Lung Carcinoma/drug therapy , Aged , ErbB Receptors/genetics , Humans , Lung Neoplasms/metabolism , Male , Small Cell Lung Carcinoma/metabolism
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