Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Jul 4;20(13):3286.
doi: 10.3390/ijms20133286.

Cutaneous Metastasis after Surgery, Injury, Lymphadenopathy, and Peritonitis: Possible Mechanisms

Affiliations
Review

Cutaneous Metastasis after Surgery, Injury, Lymphadenopathy, and Peritonitis: Possible Mechanisms

Isao Otsuka. Int J Mol Sci. .

Abstract

Cutaneous metastases from internal malignancies are uncommon. Umbilical metastasis, also known as Sister Joseph nodule (SJN), develops in patients with carcinomatous peritonitis or superficial lymphadenopathy, while non-SJN skin metastases develop after surgery, injury, and lymphadenopathy. In this review, the possible mechanisms of skin metastases are discussed. SJNs develop by the contiguous or lymphatic spread of tumor cells. After surgery and injury, tumor cells spread by direct implantation or hematogenous metastasis, and after lymphadenopathy, they spread by extranodal extension. The inflammatory response occurring during wound healing is exploited by tumor cells and facilitates tumor growth. Macrophages are crucial drivers of tumor-promoting inflammation, which is a source of survival, growth and angiogenic factors. Angiogenesis is promoted by the vascular endothelial growth factor (VEGF), which also mediates tumor-associated immunodeficiency. In the subcutaneous tissues that surround metastatic lymph nodes, adipocytes promote tumor growth. In the elderly, age-associated immunosuppression may facilitate hematogenous metastasis. Anti-VEGF therapy affects recurrence patterns but at the same time, may increase the risk of skin metastases. Immune suppression associated with inflammation may play a key role in skin metastasis development. Thus, immune therapies, including immune checkpoint inhibitors reactivating cytotoxic T-cell function and inhibiting tumor-associated macrophage function, appear promising.

Keywords: cancer; cutaneous metastasis; extranodal extension; inflammation; skin metastasis; wound healing.

PubMed Disclaimer

Conflict of interest statement

The author declares no conflict of interest.

Figures

Figure 1
Figure 1
Possible mechanisms of skin metastases. Main pathways are depicted.

References

    1. Takeo M., Lee W., Ito M. Wound Healing and Skin Regeneration. Cold Spring Harb. Perspect. Med. 2015;5:a023267. doi: 10.1101/cshperspect.a023267. - DOI - PMC - PubMed
    1. Lookingbill D.P., Spangler N., Sexton F.M. Skin involvement as the presenting sign of internal carcinoma. A retrospective study of 7316 cancer patients. J. Am. Acad. Dermatol. 1990;22:19–26. doi: 10.1016/0190-9622(90)70002-Y. - DOI - PubMed
    1. Hu S.C.S., Hen G.S., Wu C.S., Chai C.Y., Chen W.T., Lan C.C.E. Rates of cutaneous metastases from different internal malignancies: Experience from a Taiwanese medical center. J. Am. Acad. Dermatol. 2009;60:379–387. doi: 10.1016/j.jaad.2008.10.007. - DOI - PubMed
    1. Otsuka I., Matsuura T. Skin metastases in epithelial ovarian and fallopian tube carcinoma. Medicine. 2017;96:e7798. doi: 10.1097/MD.0000000000007798. - DOI - PMC - PubMed
    1. Cormio G., Capotorto M., Di Vagno G., Cazzolla A., Carriero C., Selvaggi L. Skin metastases in ovarian carcinoma: A report of nine cases and a review of the literature. Gynecol. Oncol. 2003;90:682–685. doi: 10.1016/S0090-8258(03)00400-1. - DOI - PubMed

MeSH terms