Clinical, Radiologic, and Pathologic Characteristics of Pulmonary Hamartomas With Uncommon Presentation

被引:8
作者
Chatzopoulos, Kyriakos [1 ]
Johnson, Tucker F. [2 ]
Boland, Jennifer M. [1 ]
机构
[1] Mayo Clin, Div Anat Pathol, Rochester, MN 55905 USA
[2] Mayo Clin, Div Thorac Radiol, Rochester, MN USA
关键词
Hamartoma; Lung; Radiology; Pathology; CHONDROID HAMARTOMAS; CHONDROMATOUS HAMARTOMAS; HMGI-C; LUNG; REARRANGEMENTS; MIMICKING; METASTASIS; FREQUENCY; 12Q14-15; CANCER;
D O I
10.1093/ajcp/aqaa193
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Objectives: To investigate the clinicopathologic and radiologic features of pulmonary hamartomas (PHs) with uncommon clinical presentation. Methods: A retrospective clinicopathologic and radiologic review was performed for patients diagnosed (1999-2019) with multiple hamartomas, lesions arising adjacent to a coexisting pulmonary malignancy, and tumors with predominantly extrapulmonary localization. Results: Of 979 patients diagnosed with PHs, 6 (0.6%) had multiple hamartomas, 4 (0.4%) had hamartomas adjacent to lung adenocarcinoma, and 2 (0.2%) had large mediastinal masses. Patients with multiple lesions had a median age of 65 years and mean tumor size of 0.9 cm; 1 patient had 3 hamartomas, and 5 patients had 2. Lesions next to adenocarcinomas had a mean size of 1.4 cm, and affected patients had a median age of 69 years. Predominantly mediastinal PHs, diagnosed in a 63-year-old woman and a 68-year-old man, measured 4.1 to 6 cm and were connected to the lung. All lesions were solid on imaging with absence of definitive fat or calcification, concerning for granuloma or malignancy. All cases had typical histology of PH, although one of the mediastinal tumors had an unusual amount of epithelial hyperplasia. Conclusions: PHs can be clinically and radiologically challenging to diagnose. Histopathologic examination of biopsies and resection specimens is diagnostically crucial in this setting.
引用
收藏
页码:903 / 911
页数:9
相关论文
共 65 条
  • [1] Mediastinal hamartoma - A rare presentation
    Balakrishnan, Jayaprakash
    Maniyan, Deepu
    Nayak, Nileena
    Nair, Anila Kunjulekshmi Amma Raveendran
    [J]. LUNG INDIA, 2015, 32 (06) : 665 - +
  • [2] Benign metastasizing leiomyoma: A review of current literature in respect to the time and type of previous gynecological surgery
    Barnas, Edyta
    Ksiazek, Mariusz
    Ras, Renata
    Skret, Andrzej
    Skret-Magierlo, Joanna
    Dmoch-Gajzlerska, Ewa
    [J]. PLOS ONE, 2017, 12 (04):
  • [3] Bini A, 2002, Interact Cardiovasc Thorac Surg, V1, P78, DOI 10.1016/S1569-9293(02)00058-0
  • [4] Intragenic breakpoint within RAD51L1 in a t(6;14)(p21.3;q24) of a pulmonary chondroid hamartoma
    Blank, C
    Schoenmakers, EFPM
    Rogalla, P
    Huys, EHLPG
    van Rijk, AAF
    Drieschner, N
    Bullerdiek, J
    [J]. CYTOGENETICS AND CELL GENETICS, 2001, 95 (1-2): : 17 - 19
  • [5] Pulmonary hamartoma mimicking a mediastinal cyst-like lesion in a heavy smoker
    Borghesi, Andrea
    Tironi, Andrea
    Benvenuti, Mauro Roberto
    Bertagna, Francesco
    De Leonardis, Maria Cristina
    Pezzotti, Stefania
    Bozzola, Giordano
    [J]. RESPIRATORY MEDICINE CASE REPORTS, 2018, 25 : 133 - 136
  • [6] Multiple endobronchial chondromatous hamartoma in a child
    Boshnakova, T
    Michailova, V
    [J]. EUROPEAN JOURNAL OF PEDIATRIC SURGERY, 1995, 5 (06) : 377 - 379
  • [7] Brichon P Y, 1987, Eur J Cardiothorac Surg, V1, P176, DOI 10.1016/1010-7940(87)90037-6
  • [9] Pulmonary hamartoma associated with typical carcinoid/tumorlet
    Cavazza, Alberto
    Paci, Massimiliano
    Rossi, Giulio
    [J]. VIRCHOWS ARCHIV, 2006, 449 (03) : 392 - 393
  • [10] Loss of succinate dehydrogenase B immunohistochemical expression distinguishes pulmonary chondromas from hamartomas
    Chatzopoulos, Kyriakos
    Fritchie, Karen J.
    Aubry, Marie-Christine
    Carney, J. Aiden
    Folpe, Andrew L.
    Boland, Jennifer M.
    [J]. HISTOPATHOLOGY, 2019, 75 (06) : 825 - 832