Primary endobronchial liposarcoma successfully resected via bronchoscopy: A rare case report with genetic analysis

被引:2
作者
Liu, Yuanshun [1 ,2 ]
Jiang, Hua [1 ,2 ]
Xu, Qiuran [3 ]
Zhou, Hongbin [1 ,3 ]
Li, Yaqing [1 ,3 ]
机构
[1] Peoples Hosp Hangzhou, Zhejiang Prov Peoples Hosp, Med Coll, Dept Resp Med, 158 Shangtang Rd, Hangzhou 310014, Zhejiang, Peoples R China
[2] Zhejiang Chinese Med Univ, Clin Med Coll 2, Hangzhou 310053, Zhejiang, Peoples R China
[3] Peoples Hosp Hangzhou, Zhejiang Prov Peoples Hosp, Med Coll, Key Lab Tumor Mol Diag & Individualized Med Zheji, Hangzhou 310014, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
primary endobronchial liposarcoma; atypical lipomatous tumor/well-differentiated liposarcoma; bronchoscopic surgery; murine double-minute type 2; cyclin-dependent kinase 4; WELL-DIFFERENTIATED LIPOSARCOMA; DEEP-SEATED LIPOMA; DEDIFFERENTIATED LIPOSARCOMA; PRB PHOSPHORYLATION; MDM2; CDK4; TUMORS; P16; IMMUNOHISTOCHEMISTRY; AMPLIFICATION;
D O I
10.3892/ol.2018.8737
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Liposarcoma is the most common type of soft-tissue sarcoma, and predominantly originates from the extremities and retroperitoneal cavity. However, primary endobronchial liposarcoma is extremely rare. The present study reports on the case of a 54-year-old man, a smoker, diagnosed with primary endobronchial atypical lipomatous tumor/well-differentiated liposarcoma (ALT-WDLS), which was successfully resected via bronchoscopy. Chest computed tomography (CT) revealed a neoplasm in the left main bronchus measuring 12.8x7.8 mm. Bronchoscopy demonstrated multiple roundish, pedunculated, polypoid masses in the left main bronchus. Bioptic specimens were obtained from the roundish masses, and pathological examination revealed an adipose tissue-derived tumor. The masses were completely resected during the second bronchoscopy under general anesthesia. Histopathological examination of the radical resection specimen revealed that it was an ALT-WDLS. The patient showed good quality of life at the 6-month postoperative follow-up without evidence of recurrence. Immunohistochemistry was completed with the human homologue of murine double-minute type 2 (MDM2) (+), cyclin-dependent kinase 4 (CDK4) (+), p16 (+), S-100 (+), Ki-67 (+), cluster of differentiation 34 (CD34) (+) and retinoblastoma protein (+), confirming ALT-WDLS. However, the fluorescence in situ hybridization assay revealed no amplification of MDM2 and CDK4 in the ALT-WDLS. To the best of our knowledge, the present case report is the first to describe the clinicopathologic features and genetic analysis of endobronchial liposarcoma. Although rare, this case is a reminder that clinicians should consider the possibility of this rare endobronchial tumor in patients with nonspecific symptoms including chronic cough, chest pain and recurrent pneumonia. As in this case, endoscopic treatment provided an excellent clinical outcome in patients with primary endobronchial ALT-WDLS.
引用
收藏
页码:843 / 848
页数:6
相关论文
共 26 条
  • [1] MDM2 and CDK4 immunostainings are useful adjuncts in diagnosing well-differentiated and dedifferentiated liposarcoma subtypes -: A comparative analysis of 559 soft tissue neoplasms with genetic data
    Binh, MBN
    Sastre-Garau, X
    Guillou, L
    de Pinieux, G
    Terrier, P
    Lagacé, R
    Aurias, A
    Hostein, I
    Coindre, JM
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2005, 29 (10) : 1340 - 1347
  • [2] Most malignant fibrous histiocytomas developed in the retroperitoneum are dedifferentiated liposarcomas: A review of 25 cases initially diagnosed as malignant fibrous histiocytoma
    Coindre, JM
    Mariani, O
    Chibon, F
    Mairal, A
    Somerhausen, ND
    Favre-Guillevin, E
    Bui, NB
    Stoeckle, E
    Hostein, I
    Aurias, A
    [J]. MODERN PATHOLOGY, 2003, 16 (03) : 256 - 262
  • [3] Array-based comparative genomic hybridisation analysis of a pleomorphic myxoid liposarcoma
    Creytens, David
    van Gorp, Joost
    Ferdinande, Liesbeth
    Van Roy, Nadine
    Libbrecht, Louis
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 2014, 67 (09) : 834 - +
  • [4] Incidence of Sarcoma Histotypes and Molecular Subtypes in a Prospective Epidemiological Study with Central Pathology Review and Molecular Testing
    Ducimetiere, Francoise
    Lurkin, Antoine
    Ranchere-Vince, Dominique
    Decouvelaere, Anne-Valerie
    Peoc'h, Michel
    Istier, Luc
    Chalabreysse, Philippe
    Muller, Christine
    Alberti, Laurent
    Bringuier, Pierre-Paul
    Scoazec, Jean-Yves
    Schott, Anne-Marie
    Bergeron, Christophe
    Cellier, Dominic
    Blay, Jean-Yves
    Ray-Coquard, Isabelle
    [J]. PLOS ONE, 2011, 6 (08):
  • [5] Inhibition of pRb phosphorylation and cell-cycle progression by a 20-residue peptide derived from p16(CDKN2/INK4A)
    Fahraeus, R
    Paramio, JM
    Ball, KL
    Lain, S
    Lane, DP
    [J]. CURRENT BIOLOGY, 1996, 6 (01) : 84 - 91
  • [6] Fletcher CDM, 2013, WHO classification of tumours of soft tissue and bone: WHO classification of tumours, V5
  • [7] p16 Immunohistochemistry as an Alternative Marker to Distinguish Atypical Lipomatous Tumor From Deep-seated Lipoma
    He, Mai
    Aisner, Seena
    Benevenia, Joseph
    Patterson, Francis
    Aviv, Hana
    Hameed, Meera
    [J]. APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 2009, 17 (01): : 51 - 56
  • [8] Differential diagnosis of atypical lipomatous tumor/well-differentiated liposarcoma and dedifferentiated liposarcoma: utility of p16 in combination with MDM2 and CDK4 immunohistochemistry
    Kammerer-Jacquet, Solene-Florence
    Thierry, Sixte
    Cabillic, Florian
    Lannes, Morgane
    Burtin, Florence
    Henno, Sebastien
    Dugay, Frederic
    Bouzille, Guillaume
    Rioux-Leclercq, Nathalie
    Belaud-Rotureau, Marc-Antoine
    Stock, Nathalie
    [J]. HUMAN PATHOLOGY, 2017, 59 : 34 - 40
  • [9] Successful resection of a massive mediastinal liposarcoma that rapidly extended into the entire left thoracic cavity: report of a case
    Kashu, Yasuaki
    Yukumi, Shungo
    Tsunooka, Nobuo
    Tanigawa, Kazufumi
    Arakane, Motoki
    Nakagawa, Hiromichi
    Kawachi, Kanji
    [J]. SURGERY TODAY, 2012, 42 (01) : 68 - 71
  • [10] KATO J, 1993, GENE DEV, V7, P331