Angiotropism in recurrent cutaneous squamous cell carcinoma: Implications for regional tumor recurrence and extravascular migratory spread

Extravascular migratory metastasis is a form of cancer metastasis in which tumor cells spread by tracking along the abluminal aspect of vessel walls without breaking the vascular endothelial lining or intraluminal invasion. This phenomenon has been extensively described in melanoma and is being increasingly recognized in other neoplasms. Various modalities of treatment, including radiation‐, chemo‐, targeted‐, and immune‐ therapies may potentially induce angiotropic behavior in neoplastic cells. Although there is a risk for tumor recurrence and metastasis, angiotropism may be under‐recognized and is rarely reported. Here, we report a case of recurrent poorly‐differentiated acantholytic squamous cell carcinoma of the scalp with extensive perineural invasion, previously treated with multiple therapies. There was multifocal extravascular cuffing of neoplastic cells around and focally involving the walls of small to medium‐caliber blood vessels within and surrounding the tumor, without obvious tumor intravasation. In addition, small subtle nests of neoplastic keratinocytes were noted along the abluminal aspect of a large‐caliber deep dermal blood vessel in an en‐face margin, away from the main tumor mass. Such involvement can be difficult to identify; and thus, may be missed particularly during intra‐operative frozen section evaluation, leading to false‐negative margins and is therefore, a diagnostic pitfall.

[1]  C. Stewart,et al.  Extravascular Migratory Metastasis (Pericytic Mimicry) in Sarcomatoid Squamous Cell Carcinoma of the Vulva: A Report of 2 Cases. , 2017, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

[2]  F. Del Bene,et al.  Angiotropism and extravascular migratory metastasis in cutaneous and uveal melanoma progression in a zebrafish model , 2018, Scientific Reports.

[3]  I. Oztop,et al.  Tumor deposits in salivary gland tumors , 2018, Pathology international.

[4]  S. Sarıoğlu Tumor Deposits; Mechanisms, Morphology, and Differential Diagnosis , 2018 .

[5]  F. Winkler Hostile takeover: how tumours hijack pre‐existing vascular environments to thrive , 2017, The Journal of pathology.

[6]  C. Stewart Pericytic mimicry (extravascular migratory metastasis) in neoplasia. , 2017, Human pathology.

[7]  T. Nakama,et al.  Angiotropic syringomatous carcinoma , 2017, Journal of cutaneous pathology.

[8]  S. Roman-Roman,et al.  The biological and prognostic significance of angiotropism in uveal melanoma. , 2017, Laboratory investigation; a journal of technical methods and pathology.

[9]  T. Ogawa,et al.  Acantholytic squamous cell carcinoma is usually associated with hair follicles, not acantholytic actinic keratosis, and is not “high risk”: Diagnosis, management, and clinical outcomes in a series of 115 cases , 2017, Journal of the American Academy of Dermatology.

[10]  J. Larkin,et al.  Vessel co‐option is common in human lung metastases and mediates resistance to anti‐angiogenic therapy in preclinical lung metastasis models , 2016, The Journal of pathology.

[11]  S. Dry,et al.  Pericytic mimicry in well-differentiated liposarcoma/atypical lipomatous tumor. , 2016, Human pathology.

[12]  G. Yousef,et al.  Co-option of Liver Vessels and Not Sprouting Angiogenesis Drives Acquired Sorafenib Resistance in Hepatocellular Carcinoma , 2016, Journal of the National Cancer Institute.

[13]  H. Kleinman,et al.  Imaging of Angiotropism/Vascular Co-Option in a Murine Model of Brain Melanoma: Implications for Melanoma Progression along Extravascular Pathways , 2016, Scientific Reports.

[14]  S. Sarıoğlu,et al.  Tumor deposits in head and neck carcinomas , 2016, Head & neck.

[15]  J. Landsberg,et al.  The Role of Neutrophilic Inflammation, Angiotropism, and Pericytic Mimicry in Melanoma Progression and Metastasis. , 2016, The Journal of investigative dermatology.

[16]  M. Tan,et al.  Revisiting tumor angiogenesis: vessel co-option, vessel remodeling, and cancer cell-derived vasculature formation , 2016, Chinese journal of cancer.

[17]  S. Kraft,et al.  Evaluation of frozen section margins in high‐risk cutaneous squamous cell carcinomas of the head and neck , 2015, The Laryngoscope.

[18]  S. Carmichael,et al.  Angiotropism, Pericytic Mimicry and Extravascular Migratory Metastasis in Melanoma: An Alternative to Intravascular Cancer Dissemination , 2014, Cancer Microenvironment.

[19]  M. Platten,et al.  Extravascular migratory metastasis in gynaecological carcinosarcoma , 2014, Histopathology.

[20]  D. Schadendorf,et al.  Ultraviolet-radiation-induced inflammation promotes angiotropism and metastasis in melanoma , 2014, Nature.

[21]  M. Sajin,et al.  Acantholytic squamous cell carcinoma: pathological study of nine cases with review of literature. , 2014, Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie.

[22]  H. Kleinman,et al.  Could pericytic mimicry represent another type of melanoma cell plasticity with embryonic properties? , 2013, Pigment cell & melanoma research.

[23]  R. McLendon,et al.  Glioblastoma Stem Cells Generate Vascular Pericytes to Support Vessel Function and Tumor Growth , 2013, Cell.

[24]  Matthew M. Johnson,et al.  Outcomes of primary cutaneous squamous cell carcinoma with perineural invasion: an 11-year cohort study. , 2013, JAMA dermatology.

[25]  P. Mischel,et al.  Pilot Study on “Pericytic Mimicry” and Potential Embryonic/Stem Cell Properties of Angiotropic Melanoma Cells Interacting with the Abluminal Vascular Surface , 2013, Cancer Microenvironment.

[26]  J. Wilmott,et al.  Angiotropism is an independent predictor of microscopic satellites in primary cutaneous melanoma , 2012, Histopathology.

[27]  S. Ergün,et al.  Tumor vessel stabilization and remodeling by anti-angiogenic therapy with bevacizumab , 2012, Histochemistry and Cell Biology.

[28]  A. Eggermont,et al.  Gene expression profiling of human angiotropic primary melanoma: selection of 15 differentially expressed genes potentially involved in extravascular migratory metastasis. , 2011, European journal of cancer.

[29]  R. Phelps,et al.  Histopathological Variants of Cutaneous Squamous Cell Carcinoma: A Review , 2010, Journal of skin cancer.

[30]  A. Troxel,et al.  Diameter of Involved Nerves Predicts Outcomes in Cutaneous Squamous Cell Carcinoma with Perineural Invasion: An Investigator‐Blinded Retrospective Cohort Study , 2009, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].

[31]  H. Kleinman,et al.  Overexpression of malignancy‐associated laminins and laminin receptors by angiotropic human melanoma cells in a chick chorioallantoic membrane model , 2009, Journal of cutaneous pathology.

[32]  Lizhi Zhang,et al.  Endoscopic ultrasound fine-needle aspiration detection of extravascular migratory metastasis from a remotely located pancreatic cancer. , 2009, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

[33]  R. Scolyer,et al.  Angiotropism is an Independent Predictor of Local Recurrence and In-transit Metastasis in Primary Cutaneous Melanoma , 2008, The American journal of surgical pathology.

[34]  J. Simon,et al.  Ultraviolet‐B irradiation enhances melanoma cell motility via induction of autocrine interleukin 8 secretion , 2007, Experimental dermatology.

[35]  Carter Q. Le,et al.  Angiotropism of human prostate cancer cells: implications for extravascular migratory metastasis , 2005, BJU international.

[36]  C. Lugassy,et al.  Angiotropic malignant melanoma and extravascular migratory metastasis: description of 36 cases with emphasis on a new mechanism of tumour spread , 2004, Pathology.

[37]  P. Dirks Glioma Migration: Clues from the Biology of Neural Progenitor Cells and Embryonic CNS Cell Migration , 2001, Journal of Neuro-Oncology.

[38]  C. Lugassy,et al.  Angiotropism in cutaneous melanoma: a prognostic factor strongly predicting risk for metastasis. , 2002, The Journal of investigative dermatology.

[39]  M. Westphal,et al.  Anti-VEGF antibody treatment of glioblastoma prolongs survival but results in increased vascular cooption. , 2000, Neoplasia.

[40]  C. Lugassy,et al.  Angio-tumoral complex in human malignant melanoma characterised by free laminin: ultrastructural and immunohistochemical observations. , 1997, Journal of submicroscopic cytology and pathology.

[41]  D. Brodland,et al.  The Many Faces of Squamous Cell Carcinoma , 1996, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].