Lang Yuejiao, Guo Shaolei, Tuo Ying, Tian Tian, Wang Yuefeng, Li Qiming, Chen Yingqian, Chen Wenli, Zhu Yonghong, Liu Dawei
Departments of Pathology.
Neurosurgery.
Am J Surg Pathol. 2025 Mar 1;49(3):243-250. doi: 10.1097/PAS.0000000000002339. Epub 2024 Dec 17.
Immature PIT1-lineage pituitary neuroendocrine tumors (PitNETs)/adenomas (Immature PIT1-lineage tumors) are a rare and underrecognized subtype of PitNETs that exhibits distinct cytologic atypia features and aggressive clinical potential. This study characterizes the clinical, radiological, histologic, and immunohistochemical features of 15 immature PIT1-lineage tumors identified from 1084 PitNETs patients over 5 years. Our cohort of 6 males and 9 females had a median age of 37.00 years (range: 23 to 68 y). All patients presented with pituitary macrotumors with an average size of 27.13×22.60×22.13 mm (length×width×height). The invasive growth pattern was identifiable, with 40.00% of tumors presenting with advanced stage (Knosp type 3 and 4) disease, followed by 20.00% Knosp type 2, 26.67% type 1, and 13.33% type 0. Clinical follow-up in 11 patients (median duration: 10.91 mo) revealed local recurrence in 1 case (9.09%). Microscopically, immature PIT1-lineage tumors comprised epithelioid (n=14) or spindle-shaped (n=1) chromophobic or weak basophilic cells with marked cytologic atypia, macronucleoli, and nuclear pseudoinclusions. By immunohistochemistry, most cases showed a consistent stain for PIT1 but limited expression of PIT1 family hormones in conjunction with diffuse or focal expression of CK8/18 (Cam 5.2), whereas none of the mimics showed a similar stain pattern in such a distinct way. We corroborate that immature PIT1-lineage tumors are rare, aggressive, and morphologically unique PitNETs/adenomas with cytologic atypia features. Immunohistochemistry may facilitate diagnosis in the distinction from histologic mimics.
未成熟的PIT1谱系垂体神经内分泌肿瘤(PitNETs)/腺瘤(未成熟的PIT1谱系肿瘤)是PitNETs中一种罕见且未被充分认识的亚型,具有独特的细胞学异型性特征和侵袭性临床潜能。本研究对5年期间从1084例PitNETs患者中识别出的15例未成熟PIT1谱系肿瘤的临床、放射学、组织学和免疫组化特征进行了描述。我们的队列中有6名男性和9名女性,中位年龄为37.00岁(范围:23至68岁)。所有患者均表现为垂体大肿瘤,平均大小为27.13×22.60×22.13mm(长×宽×高)。侵袭性生长模式可识别,40.00%的肿瘤表现为晚期(Knosp 3型和4型)疾病,其次是20.00%的Knosp 2型、26.67%的1型和13.33%的0型。对11例患者的临床随访(中位持续时间:10.91个月)显示1例(9.09%)局部复发。显微镜下,未成熟的PIT1谱系肿瘤由上皮样(n = 14)或梭形(n = 1)嫌色或弱嗜碱性细胞组成,具有明显的细胞学异型性、大核仁和核假包涵体。通过免疫组化,大多数病例对PIT1呈一致染色,但PIT1家族激素表达有限,同时CK8/18(Cam 5.2)呈弥漫性或局灶性表达,而模拟物均未以如此独特的方式呈现类似的染色模式。我们证实未成熟的PIT1谱系肿瘤是罕见的、侵袭性的且形态学上独特的PitNETs/腺瘤,具有细胞学异型性特征。免疫组化可能有助于与组织学模拟物进行鉴别诊断。