Imaging of renal medullary carcinoma in children and young adults: a report from the Children's Oncology Group

被引:13
作者
Sandberg, Jesse K. [1 ]
Mullen, Elizabeth A. [2 ]
Cajaiba, Mariana M. [3 ]
Smith, Ethan A. [4 ]
Servaes, Sabah [5 ]
Perlman, Elizabeth J. [3 ]
Geller, James I. [6 ]
Ehrlich, Peter F. [7 ]
Cost, Nicholas G. [8 ]
Dome, Jeffrey S. [9 ]
Fernandez, Conrad V. [10 ,11 ]
Khanna, Geetika [1 ]
机构
[1] Washington Univ, Sch Med, Mallinckrodt Inst Radiol, 510 S Kingshighway,Campus Box 8131, St Louis, MO 63110 USA
[2] Childrens Hosp, Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Northwestern Univ, Feinberg Sch Med, Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pathol & Lab Med, Chicago, IL 60611 USA
[4] Univ Michigan Hlth Syst, Dept Radiol, Sect Pediat Radiol, CS Mott Childrens Hosp, Ann Arbor, MI USA
[5] Childrens Hosp Philadelphia, Dept Radiol, Philadelphia, PA 19104 USA
[6] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Div Pediat Oncol, Cincinnati, OH USA
[7] Univ Michigan Hlth Syst, Dept Surg, Pediat Surg Sect, CS Mott Childrens Hosp, Ann Arbor, MI USA
[8] Univ Colorado, Sch Med, Dept Surg, Div Urol, Aurora, CO USA
[9] Childrens Natl Med Ctr, Div Pediat Oncol, Washington, DC 20010 USA
[10] Dalhousie Univ, Dept Pediat, Halifax, NS, Canada
[11] IWK Hlth Ctr, Halifax, NS, Canada
关键词
Children; Computed tomography; Lymphangitic carcinomatosis; Medullary carcinoma; Renal tumor; Sickle cell; SICKLE-CELL TRAIT; TUMORS; CT; FEATURES;
D O I
10.1007/s00247-017-3926-6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To characterize the clinical and imaging features of pediatric renal medullary carcinoma at initial presentation. We retrospectively analyzed images of 25 pediatric patients with renal medullary carcinoma enrolled in the Children's Oncology Group renal tumors classification, biology and banking study (AREN03B2) from March 2006 to August 2016. Imaging findings of the primary mass, and patterns of locoregional and distant spread were evaluated in correlation with pathological and surgical findings. Median age at presentation was 13 years (range: 6-21 years), with a male predominance (3.2:1). The overall stage of disease at initial presentation was stage 1 in 1, stage 2 in 2 and stage 4 in 22. Maximum diameter of the primary renal mass ranged from 1.6 to 10.3 cm (mean: 6.6 cm) with a slight right side predilection (1.5:1). Enlarged (> 1 cm short axis) retroperitoneal lymph nodes were identified at initial staging in 20/25 (80%) cases, 10 of which were histologically confirmed while the others did not undergo surgical sampling. Enlarged lymph nodes were also identified in the mediastinum (14/25; 56%) and supraclavicular regions (4/25; 16%). Metastatic disease was present in the lungs in 19/25 (76%) and liver in 6/25 (24%). The pattern of lung metastases was pulmonary lymphangitic carcinomatosis: 10 cases (9 bilateral, 1 unilateral), pulmonary nodules with indistinct margins: 6 cases, pulmonary nodules with distinct margins: 2 cases, while 1 case had pulmonary nodules with both indistinct and distinct margins. Pulmonary lymphangitic carcinomatosis was pathologically confirmed in 4/10 cases. All cases with pulmonary lymphangitic carcinomatosis had associated enlarged mediastinal lymph nodes. Renal medullary carcinoma in children and young adults presents at an advanced local and distant stage in the majority of patients. The diagnosis of renal medullary carcinoma should be considered when a child or young adult presents with a poorly defined/infiltrative, centrally located renal mass, especially in the setting of known sickle cell hemoglobinopathy. Distant metastases are common at initial presentation in the lungs, distant lymph nodes and liver and often involve multiple sites simultaneously. Pulmonary lymphangitic carcinomatosis, a distinctive and uncommon form of lung metastasis in children, is common in this patient population.
引用
收藏
页码:1615 / 1621
页数:7
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