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J Vet Diagn Invest. 2022 May;34(3):535-538. doi: 10.1177/10406387221081435. Epub 2022 Mar 15.
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Review of Histological Grading Systems in Veterinary Medicine.兽医组织学分级系统综述。
Vet Pathol. 2021 Sep;58(5):809-828. doi: 10.1177/0300985821999831. Epub 2021 Mar 26.
2
Unilateral renal cystadenocarcinoma and nodular dermatofibrosis in a mixed-breed dog carrying a FLCN gene mutation.一只携带FLCN基因突变的混种犬出现单侧肾囊肿腺癌和结节性皮肤纤维瘤。
Vet Dermatol. 2019 Jan 23. doi: 10.1111/vde.12719.
3
Primary Meningeal Rhabdomyosarcoma of the Spinal Cord of a Young Dog with Neuromelanocytosis and Multiple Cutaneous Neurofibromas.一只患有神经黑素沉着症和多发性皮肤神经纤维瘤的幼犬脊髓原发性脑膜横纹肌肉瘤
J Comp Pathol. 2018 Nov;165:57-61. doi: 10.1016/j.jcpa.2018.09.008. Epub 2018 Oct 25.
4
Malignant Cutaneous Peripheral Nerve Sheath Tumour with Rhabdomyosarcomatous Differentiation (Triton Tumour) in a Domestic Cat.一只家猫身上的具有横纹肌肉瘤分化的恶性皮肤周围神经鞘瘤(蝾螈瘤)
J Comp Pathol. 2018 Nov;165:1-5. doi: 10.1016/j.jcpa.2018.09.003. Epub 2018 Oct 18.
5
Endocardial Peripheral Nerve Sheath Tumour with Features of a Benign Schwannoma in a Donkey.一头驴身上具有良性神经鞘瘤特征的心内膜周围神经鞘瘤
J Comp Pathol. 2017 Nov;157(4):280-283. doi: 10.1016/j.jcpa.2017.09.003. Epub 2017 Oct 21.
6
Neurofibromatosis type 1: a multidisciplinary approach to care.神经纤维瘤病 1 型:多学科护理方法。
Lancet Neurol. 2014 Aug;13(8):834-43. doi: 10.1016/S1474-4422(14)70063-8.
7
Prognostic factors for cutaneous and subcutaneous soft tissue sarcomas in dogs.犬皮肤和皮下软组织肉瘤的预后因素。
Vet Pathol. 2011 Jan;48(1):73-84. doi: 10.1177/0300985810388820. Epub 2010 Dec 7.
8
Malignant peripheral nerve sheath tumor associated with neurofibromatosis type 1, with metastasis to the heart: a case report.1 型神经纤维瘤病相关的恶性外周神经鞘瘤伴心脏转移:病例报告。
Diagn Pathol. 2010 Jan 9;5:2. doi: 10.1186/1746-1596-5-2.
9
Localized, plexiform, diffuse, and other variants of neurofibroma in 12 dogs, 2 horses, and a chicken.12只犬、2匹马和1只鸡身上出现的局限性、丛状、弥漫性及其他神经纤维瘤变体。
Vet Pathol. 2009 Sep;46(5):904-15. doi: 10.1354/vp.08-VP-0322-S-FL. Epub 2009 May 9.
10
Immunoreactivity of bovine schwannomas.牛神经鞘瘤的免疫反应性。
J Comp Pathol. 2007 Nov;137(4):224-230. doi: 10.1016/j.jcpa.2007.07.003. Epub 2007 Sep 21.

具有外周神经鞘瘤特征的皮肤梭形细胞肿瘤,并伴有心脏受累:拉布拉多猎犬犬中类似于神经纤维瘤病 1 型的表现。

Cutaneous spindle cell tumors with features of peripheral nerve sheath tumors and concurrent cardiac involvement: neurofibromatosis type 1-like presentation in a Labrador Retriever dog.

机构信息

Idexx Laboratories Italia, Milan, Italy.

Clinica Veterinaria Monte Rosa, Castelletto Sopra Ticino (NO), Italy.

出版信息

J Vet Diagn Invest. 2022 May;34(3):535-538. doi: 10.1177/10406387221081435. Epub 2022 Mar 15.

DOI:10.1177/10406387221081435
PMID:35291897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9254057/
Abstract

An 8-y-old intact male Labrador Retriever dog developed cutaneous masses over the entire body. On histologic evaluation, the masses were composed of bundles of fusiform neoplastic cells arranged around adnexa, with mild atypia and no mitoses, consistent with peripheral nerve sheath tumors (PNSTs). Immunohistochemically, neoplastic cells were immunoreactive for vimentin, glial fibrillary acidic protein (GFAP), and S100, confirming their perineurial origin. The dog was euthanized because of deteriorating clinical signs. In addition to the cutaneous masses, a cardiac mass was identified at postmortem examination. The histopathologic and immunohistochemical features of the cardiac mass were similar to those of the cutaneous masses. To our knowledge, the combination of multiple cutaneous masses with features of PNSTs and a concurrent cardiac lesion has not been reported previously in a dog. We suggest "neurofibromatosis type 1-like" presentation for this unique combination of cutaneous and cardiac masses. Further studies are required to investigate the etiopathogenesis of this condition and explore its genetic background.

摘要

一只 8 岁的雄性完整拉布拉多猎犬犬全身出现皮肤肿块。组织学评估显示,这些肿块由围绕附属物排列的束状梭形肿瘤细胞组成,具有轻度异型性,没有有丝分裂,符合外周神经鞘肿瘤(PNST)的特征。免疫组化染色显示,肿瘤细胞对波形蛋白、神经胶质纤维酸性蛋白(GFAP)和 S100 呈阳性反应,证实其为神经鞘起源。由于临床症状恶化,这只狗被实施了安乐死。除了皮肤肿块外,尸检还发现了一个心脏肿块。心脏肿块的组织病理学和免疫组化特征与皮肤肿块相似。据我们所知,以前在犬中尚未报道过具有 PNST 特征的多发性皮肤肿块和同时存在的心脏病变的情况。我们建议将这种独特的皮肤和心脏肿块组合归类为“1 型神经纤维瘤病样”表现。需要进一步的研究来探讨这种情况的病因发病机制,并探索其遗传背景。