Flores Laura, Sleightholm Richard, Neilsen Beth, Baine Michael, Drincic Andjela, Thorell William, Shonka Nicole, Oupicky David, Zhang Chi
College of Allied Health Professionals, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Case Rep Oncol. 2019 Feb 8;12(1):139-146. doi: 10.1159/000496019. eCollection 2019 Jan-Apr.
Pituitary tumors typically remain silent unless interaction with nearby structures occurs. Rare subsets of pituitary tumors display aggressive phenotypes: highly mitotic, locally invasive, metastatic, chemotherapy and radiation resistant, etc. Disease progression and response to therapy is ill-defined in these subtypes, and their true prognostic potential is debated. Thus, identifying tumor characteristics with prognostic value and efficacious treatment options remains a challenge in aggressive pituitary tumors.
A 45-year-old female presented with a nonfunctioning corticotropic pituitary macroadenoma with biomarkers suggestive of an "atypical" subtype: Ki-67 of 8-12%, increased mitosis, and locally invasive. Despite resections and radiation, growth continued, eventually affecting her vision. Although histologically ACTH positive, the patient remained clinically asymptomatic. Twelve months later, an episode of Cushing's disease-induced psychosis prompted a PET-CT scan, identifying sites of metastasis. Temozolomide was added to her medical regimen, and her metastatic liver lesions and boney metastases were treated with radiofrequency ablation and stereotactic body radiation therapy, respectively. Systemic treatment resulted in a drop in her ACTH levels, with her most recent scans/labs at 12 months following RFA suggesting remission.
This is a unique presentation of a pituitary tumor, displaying characteristics of both clinically silent corticotropic and "atypical" macroadenoma subtypes. Although initially ACTH positive while clinically silent, the patient's disease ultimately recurred metastatically with manifestations of Cushing's disease and psychosis. With the addition of temozolomide to her treatment plan, her primary and metastatic sites have responded favorably to radiation therapy. Thus, the addition of temozolomide may be beneficial in the treatment of aggressive pituitary tumors.
垂体瘤通常无症状,除非与附近结构发生相互作用。垂体瘤的罕见亚群表现出侵袭性表型:高有丝分裂、局部侵袭、转移、对化疗和放疗耐药等。这些亚群的疾病进展和对治疗的反应尚不明确,其真正的预后潜力也存在争议。因此,在侵袭性垂体瘤中,识别具有预后价值的肿瘤特征和有效的治疗方案仍然是一项挑战。
一名45岁女性患有无功能促肾上腺皮质激素垂体大腺瘤,其生物标志物提示为“非典型”亚群:Ki-67为8-12%,有丝分裂增加,且局部侵袭。尽管进行了手术切除和放疗,但肿瘤仍继续生长,最终影响了她的视力。尽管组织学上促肾上腺皮质激素呈阳性,但患者临床上仍无症状。12个月后,库欣病诱发的精神病发作促使进行了PET-CT扫描,发现了转移部位。替莫唑胺被添加到她的治疗方案中,她的肝脏转移灶和骨转移分别接受了射频消融和立体定向体部放射治疗。全身治疗导致她的促肾上腺皮质激素水平下降,射频消融后12个月的最新扫描/检查结果显示病情缓解。
这是垂体瘤的一种独特表现,兼具临床无症状促肾上腺皮质激素型和“非典型”大腺瘤亚群的特征。尽管最初促肾上腺皮质激素呈阳性但临床上无症状,但患者的疾病最终发生了转移复发,出现了库欣病和精神病的表现。在她的治疗方案中添加替莫唑胺后,她的原发部位和转移部位对放疗反应良好。因此,添加替莫唑胺可能对侵袭性垂体瘤的治疗有益。