1.Progress on the Study of Tumor Spread Through Air Spaces in the Clinicopathological Characteristics of Lung Adenocarcinoma and Its Influence on the Surgical Treatment and Prognosis of Lung Cancer.
Chinese Journal of Lung Cancer 2019;22(6):363-368
Tumor spread through air spaces (STAS) as a new pathological invasion mode is closely related to many clinicopathological factors. In lung adenocarcinoma, micropapillary and solid pathological subtypes are most related; STAS for early stage lung adenocarcinoma, surgical type of lobectomy seems to benefit better than sublobar resection, which may up-regulate the pathological stage of early lung cancer; Moreover, STAS is closely related to squamous cell carcinoma and other non-small cell lung cancer (NSCLC). In addition, intraoperative frozen-section pathological detection of STAS is difficult and controversial. STAS as an independent risk factor for tumor recurrence is also an important factor indicating poor prognosis. This paper reviews the research status and progress of STAS.
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Adenocarcinoma of Lung
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diagnosis
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pathology
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surgery
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Animals
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Humans
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Lung Neoplasms
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diagnosis
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pathology
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surgery
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Neoplasm Invasiveness
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Prognosis
2.Pulmonary Pleomorphic Adenoma: Report of a Rare Case.
The Korean Journal of Internal Medicine 2007;22(2):122-124
Primary pleomorphic adenoma of the lung is a type of pulmonary adenoma that is extremely rare, and it predominantly occurs in the proximal airway. We recently experienced a case of a peripheral solitary pulmonary nodule that was discovered on the CT scans. We performed wedge resection with video-assisted thoracoscopic surgery and we firmly diagnosed this lesion as pulmonary pleomorphic adenoma according to the histology. We report here on a rare benign tumor that was diagnosed as a primary pleomorphic adenoma located in the lung periphery.
Adenoma, Pleomorphic/*diagnosis/pathology/surgery
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Adult
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Female
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Humans
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Lung Neoplasms/*diagnosis/pathology/surgery
3.Benign Pulmonary Metastasizing Leiomyomatosis: Case Report and a Review of the Literature.
Young Il KWON ; Tae Hyung KIM ; Jang Won SOHN ; Ho Joo YOON ; Dong Ho SHIN ; Sung Soo PARK
The Korean Journal of Internal Medicine 2006;21(3):173-177
The authors report here on a case of a nearly asymptomatic 51-year-old Korean woman who was found to have diffuse, multiple nodules of the lungs on a routine chest radiograph. She had undergone hysterectomy 16 years previously for uterine myoma. An open lung biopsy revealed tumor that was composed of interlacing bundles of spindle cells with cigar shaped nucleus and eosinophilic myofibrils in the cytoplasm; consistent with multiple leiomyomas. The stains for SMA, desmin, MSA and Ki-67 were positive and the stain for c-kit was negative. The other stains for estrogen and progesterone receptor were positive. During the open lung biopsy procedure, all the nodules were excised. We report here on an interesting case of benign metastasizing leiomyoma (BML) in 51-year-old patient. To the best of our knowledge, this case showed the longest period of clinical progression in Korea. This is also one of a few cases in which curative excision was successfully performed.
Uterine Neoplasms/*pathology/surgery
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Ovariectomy
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Middle Aged
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Lung Neoplasms/diagnosis/*secondary
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Leiomyomatosis/*pathology/surgery
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Hysterectomy
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Humans
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Female
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Disease Progression
4.Primary pulmonary rhabdomyosarcoma in children: report of 1 case.
Jiaosheng ZHANG ; Yanxia HE ; Weiguo YANG ; Yuejie ZHENG ; Yimei DONG
Chinese Journal of Pediatrics 2014;52(6):475-476
Biopsy
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Bronchial Neoplasms
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diagnosis
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pathology
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surgery
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Bronchoscopy
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Child
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Diagnosis, Differential
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Fatal Outcome
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Female
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Humans
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Lung
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diagnostic imaging
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surgery
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Lung Neoplasms
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diagnosis
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pathology
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surgery
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Neoplasm Metastasis
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Rhabdomyosarcoma, Embryonal
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diagnosis
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pathology
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surgery
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Tomography, X-Ray Computed
5.A Case of Lambert-Eaton Myasthenic Syndrome Associated with Atypical Bronchopulmonary Carcinoid Tumor.
Jae Hyeok LEE ; Jin Hong SHIN ; Dae Seong KIM ; Dae Soo JUNG ; Kyu Hyun PARK ; Min Ki LEE ; Jee Yeon KIM
Journal of Korean Medical Science 2004;19(5):753-755
The Lambert-Eaton myasthenic syndrome (LEMS) is typically recognized as a paraneoplastic syndrome associated with a small cell lung carcinoma (SCLC), whereas LEMS with other neuroendocrine lung tumors, including carcinoids or large cell lung carcinoma, are highly unusual. Here, we report a rare case of LEMS with atypical bronchopulmonary carcinoid tumor: A 65-yr-old man presented with progressive leg weakness and a diagnosis of LEMS was made by serial repetitive nerve stimulation test. Chest CT revealed a lung nodule with enlargement of paratracheal lymph nodes, and surgically resected lesion showed pathological features of atypical carcinoid tumor. We concluded that LEMS could be associated with rare pulmonary neuroendocrine tumor other than SCLC, which necessitates pathologic confirmation followed by aggressive treatment for optimal management in these rare cases.
Aged
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Carcinoid Tumor/*complications/pathology/surgery
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Electromyography
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Humans
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Lambert-Eaton Myasthenic Syndrome/*complications/diagnosis
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Lung Neoplasms/*complications/pathology/surgery
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Male
6.The Sino-French 2012 Conference in Thoracic Oncology: an international academic platform for in-depth exchange on comprehensive research.
Dong-Rong SITU ; Philippe DARTEVELLE ; Thierry Le CHEVALIER ; Lan-Jun ZHANG
Chinese Journal of Cancer 2013;32(2):53-58
The Sino-French 2012 Conference in Thoracic Oncology, held November 17-18, 2012, was hosted by the Department of Thoracic Surgery at Sun Yat-sen University Cancer Center and organized in collaboration with two prestigious French hospitals: Institute Gustave Roussy and Marie Lannelongue Hospital. The conference was established by leading experts from China and France to serve as an international academic platform for sharing novel findings in basic research and valuable clinical practice experiences. Hot topics including innovation in surgical techniques, diagnosis and staging of early-stage lung cancer, minimally invasive surgery, multidisciplinary treatment of lung cancer, and progress in radiotherapy for lung cancer were explored. Highlights of the conference presentations are summarized in this report.
Carcinoma, Non-Small-Cell Lung
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diagnosis
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pathology
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surgery
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China
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Combined Modality Therapy
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France
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Humans
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Lung Neoplasms
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diagnosis
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pathology
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surgery
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Neoplasm Staging
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Societies, Medical
7.Pleuropulmonary blastoma in an adult women with pleurorrhea as the major clinical manifestation: report of a case.
Ai-hua LIU ; Wei-yang ZHENG ; Lei WU
Journal of Southern Medical University 2008;28(12):2241-2243
Pleuropulmonary blastoma (PPB) is a rare dysontogenetic neoplasm in children and has been recognized as a distinct clinicopathological entity different from the ordinary pulmonary blastoma of adulthood. We report a very rare adult case of PPB. A 43-year-old female patient presented with massive pleural infusion, and a misdiagnosis of pleural tuberculosis (TB) was made on the basis of ultrasound scan and CT images, for which therapy with TB drugs was administered for 3 weeks. Subsequent operation and pathologic examination of the mass revealed a multicystic neoplasm consisting of malignant mesenchymal cells immunohistochemically positive for vimentin and actin. Local recurrence occurred in the left pleural 20 months after the surgical tumor resection and 4 cycles of adjuvant chemotherapy.
Adult
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Diagnosis, Differential
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Female
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Humans
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Lung Neoplasms
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diagnosis
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pathology
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surgery
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Pleural Effusion
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diagnosis
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etiology
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Pulmonary Blastoma
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diagnosis
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pathology
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surgery
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Tomography, X-Ray Computed
8.Prognosis of Non-Small Cell Lung Cancer with Synchronous Brain Metastases Treated with Gamma Knife Radiosurgery.
Doo Sik KONG ; Jung Il LEE ; Do Hyun NAM ; Kwan PARK ; Jong Hyun KIM ; Jhin Gook KIM ; Jun O PARK ; Keunchil PARK
Journal of Korean Medical Science 2006;21(3):527-532
The clinical outcome and prognostic factors of patients with synchronous brain metastases from non-small cell lung cancer (NSCLC) who were treated with gamma knife radiosurgery (GKS) were analyzed. A total of 35 patients with NSCLC underwent GKS as an initial treatment for metastatic brain lesions of synchronous onset. The period of survival and various prognostic factors such as age, gender, performance status, multiplicity of the brain lesions, intracranial tumor volume, and extent of the primary tumor were analyzed. The overall median survival time for this series was 12 months (range 0.75 to 43 months) from the diagnosis. Of the 21 patients who were no longer alive at the conclusion of this study, only 7 (33.3%) died of neurological causes. Multivariate analysis of these data revealed that N stage, whole-brain radiotherapy (WBRT), and chemotherapy were significant predictors for survival (p<0.05). Survival of patients with NSCLC and synchronous brain metastases is mainly dependent upon the progression of the systemic disease, provided that the cerebral lesions are treated adequately with local treatment modalities including radiosurgery. Application of radiosurgery as an initial treatment option and aggressive local and systemic modalities to control extracranial disease may improve survival.
Treatment Outcome
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Time Factors
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Radiosurgery/*methods
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Prognosis
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Neoplasm Metastasis
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Middle Aged
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Male
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Lung Neoplasms/*diagnosis/pathology/*surgery
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Humans
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Female
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Carcinoma, Non-Small-Cell Lung/*diagnosis/pathology/*surgery
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Brain Neoplasms/*diagnosis/pathology/*surgery
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Aged, 80 and over
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Aged
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Adult
9.Diagnosis and surgical treatment of metachronous second primary lung cancer.
Fei-yue FENG ; De-chao ZHANG ; Xiang-yang LIU ; Yong-gang WANG ; You-sheng MAO
Chinese Journal of Surgery 2005;43(6):348-350
OBJECTIVETo review the experience of the diagnosis, surgical treatment and prognosis of metachronous second primary lung cancers.
METHODSBetween January 1983 and April 2004, 32 patients with metachronous second primary lung cancers were operated in our department. Clinical data of all these patients were reviewed retrospectively.
RESULTSThe initial procedures for their first primary lung cancers were lobectomy or pneumonectomy. Lobectomy or completion pneumonectomy for the second primary lung cancers were performed in 17 cases, limited pulmonary resection was done in 14 cases and exploration was in 1 case. The postoperative morbidity and mortality were 12% (4/32) and 3% (1/32), respectively. The 1-, 3-, and 5-year survival rate after second operation were 66% (19/29), 32% (9/28) and 19% (4/21), respectively.
CONCLUSIONSThe incidence of metachronous second primary lung cancers has been increasing gradually during recent years. The closely follow-up for patients undergoing resection for their first primary lung cancers is most important factor for improvement of the diagnosis of metachronous second primary lung cancers. Limited resection and incomplete lymph node dissection might be the factors contributing to the poor prognosis.
Adult ; Aged ; Female ; Humans ; Lung Neoplasms ; diagnosis ; mortality ; pathology ; surgery ; Lymph Node Excision ; Male ; Middle Aged ; Neoplasms, Second Primary ; diagnosis ; mortality ; pathology ; surgery ; Pneumonectomy ; methods ; Prognosis ; Retrospective Studies
10.Aggressive Angiomyxoma: an Unusual Presentation.
Junzu GENG ; Bofeng CAO ; Liping WANG
Korean Journal of Radiology 2012;13(1):90-93
Aggressive angiomyxoma is an uncommon mesenchymal myxoid tumor that is characterized by slow growth and frequent local recurrence. It is currently regarded as a nonmetastasizing tumor. We describe a case of recurrent aggressive angiomyxoma with invasion into the veins including the inferior vena cava and the right atrium and with pulmonary metastases. Our case, together with those unusual cases documented in previous reports, may lead to a reappraisal of the nature of aggressive angiomyxoma.
Adult
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Biopsy
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Contrast Media/diagnostic use
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Diagnosis, Differential
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Female
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Humans
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Immunohistochemistry
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Lung Neoplasms/*secondary/surgery
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Myxoma/*diagnosis/pathology/surgery
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Radiography, Interventional
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Tomography, X-Ray Computed
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Vascular Neoplasms/*diagnosis/pathology/surgery
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Vena Cava, Inferior/pathology/surgery