glomangiosarcoma

{{short description|Cancer originating in glomus bodies}}

{{Infobox medical condition (new)

| name = Glomangiosarcoma

| synonyms = Malignant glomus tumor

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| field = Dermatology

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Glomangiosarcoma is a low grade{{cite journal |vauthors=Pérez de la Fuente T, Vega C, Gutierrez Palacios A, Sanchez Lorenzo J, Gonzalez Sarasua J |title=Glomangiosarcoma of the hypothenar eminence: a case report |journal=Chirurgie de la Main |volume=24 |issue=3–4 |pages=199–202 |year=2005 |pmid=16121631 |doi= 10.1016/j.main.2005.06.006}} tumor of the soft tissue. They rarely metastasize,{{cite journal |vauthors=Park JH, Oh SH, Yang MH, Kim NI |title=Glomangiosarcoma of the hand: a case report and review of the literature |journal=The Journal of Dermatology |volume=30 |issue=11 |pages=827–33 |date=November 2003 |pmid=14684942 |doi=10.1111/j.1346-8138.2003.tb00486.x |s2cid=21334564 |url=http://www.dermatol.or.jp/Journal/JD/2003/030110827.html |access-date=2008-10-17 |archive-url=https://web.archive.org/web/20110722120747/http://www.dermatol.or.jp/Journal/JD/2003/030110827.html |archive-date=2011-07-22 |url-status=dead |url-access=subscription }} but metastases are possible.{{cite journal |vauthors=Watanabe K, Sugino T, Saito A, Kusakabe T, Suzuki T |title=Glomangiosarcoma of the hip: report of a highly aggressive tumour with widespread distant metastases |journal=British Journal of Dermatology |volume=139 |issue=6 |pages=1097–101 |date=December 1998 |pmid=9990381 |doi=10.1046/j.1365-2133.1998.02574.x |s2cid=34576130 }} It is also known as malignant glomus tumor.{{cite journal |vauthors=Kayal JD, Hampton RW, Sheehan DJ, Washington CV |title=Malignant glomus tumor: a case report and review of the literature |journal=Dermatologic Surgery |volume=27 |issue=9 |pages=837–40 |date=September 2001 |pmid=11553174 |doi=10.1097/00042728-200109000-00011 }} Positive staining for vimentin has been reported.{{cite journal |vauthors=Hiruta N, Kameda N, Tokudome T, etal |title=Malignant glomus tumor: a case report and review of the literature |journal=The American Journal of Surgical Pathology |volume=21 |issue=9 |pages=1096–103 |date=September 1997 |pmid=9298887 |doi= 10.1097/00000478-199709000-00015}}

Signs and symptoms

Glomangiosarcoma usually manifest as painful blue-red dermal nodules that range from 0.5-2cm in size.

Causes

Glomangiosarcomas can arise de novo or from a preexisting benign glomus tumour.{{cite journal | last1=EW | first1=Gould | last2=JC | first2=Manivel | last3=J | first3=Albores-Saavedra | last4=H | first4=Monforte | title=Locally infiltrative glomus tumors and glomangiosarcomas. A clinical, ultrastructural, and immunohistochemical study | journal=Cancer | date=1990 | volume=65 | issue=2 | pages=310–318 | issn=0008-543X | pmid=2153045 | doi=10.1002/1097-0142(19900115)65:2<310::aid-cncr2820650221>3.0.co;2-q |url=https://pubmed.ncbi.nlm.nih.gov/2153045/ | access-date=2024-04-27 }}

Diagnosis

Typically, a definitive diagnosis cannot be made based solely on radiologic findings and clinical symptoms.{{cite journal | last1=Alhroub | first1=Omar A | last2=Mahameed | first2=Shimaa A | last3=Abdelhafez | first3=Mohammad O | last4=Alhroub | first4=Asil | last5=Hour | first5=Hani | last6=Hasasna | first6=Nabil | last7=Kamal | first7=Nazmi | title=A case of malignant glomus tumor (glomangiosarcoma) of the nasal cavity | journal=Journal of Surgical Case Reports | volume=2022 | issue=1 | date=2022-01-01 | pages=rjab641 | issn=2042-8812 | pmid=35096369 | pmc=8791658 | doi=10.1093/jscr/rjab641 }} To get a conclusive diagnosis of glomangiosarcoma, immunohistochemical staining in addition to hematoxylin and eosin staining is needed.{{cite journal | last1=Wang | first1=Yingjie | last2=Xiang | first2=Yongbo | last3=Bian | first3=Yanyan | last4=Feng | first4=Bin | last5=Liu | first5=Yong | last6=Zhou | first6=Xi | last7=Zhou | first7=Lizhi | last8=Weng | first8=Xisheng | title=Glomus tumors associated with the bone and joints: a review of 91 cases | journal=Annals of Translational Medicine | publisher=AME Publishing Company | volume=8 | issue=21 | year=2020 | issn=2305-5839 | doi=10.21037/atm-20-6998 | doi-access=free | pages=1460| pmid=33313205 | pmc=7723542 }}

Histologically, glomangiosarcomas differ from benign glomus tumors in that they include sheets of uniform, round to oval cells with eosinophilic cytoplasm, many vascular spaces, and cellular pleomorphism linked to frequent mitotic figures.{{cite journal | last1=Folpe | first1=Andrew L. | last2=Fanburg–Smith | first2=Julie C. | last3=Miettinen | first3=Markku | last4=Weiss | first4=Sharon W. | title=Atypical and Malignant Glomus Tumors | journal=The American Journal of Surgical Pathology | publisher=Ovid Technologies (Wolters Kluwer Health) | volume=25 | issue=1 | year=2001 | issn=0147-5185 | doi=10.1097/00000478-200101000-00001 | pages=1–12| pmid=11145243 }}

Glomangiosarcomas display many of the same antigens as their benign counterparts on immunohistochemical labeling; these antigens include vimentin, smooth muscle actin, and muscle-specific actin.{{cite journal | last1=Maselli | first1=Amy M. | last2=Jambhekar | first2=Amani V. | last3=Hunter | first3=John G. | title=Glomangiosarcoma Arising from a Prior Biopsy Site | journal=Plastic and Reconstructive Surgery — Global Open | publisher=Ovid Technologies (Wolters Kluwer Health) | volume=5 | issue=1 | year=2017 | issn=2169-7574 | doi=10.1097/gox.0000000000001219 | page=e1219| pmid=28203514 | pmc=5293312 }} On the other hand, benign tumors stain more highly for actin and myosin, and malignant tumors stain more intensely for vimentin.{{cite journal | last1=M | first1=Aiba | last2=A | first2=Hirayama | last3=S | first3=Kuramochi | title=Glomangiosarcoma in a glomus tumor. An immunohistochemical and ultrastructural study | journal=Cancer | date=1988 | volume=61 | issue=7 | pages=1467–1471 | issn=0008-543X | pmid=2449949 | doi=10.1002/1097-0142(19880401)61:7<1467::aid-cncr2820610733>3.0.co;2-3 |url=https://pubmed.ncbi.nlm.nih.gov/2449949/ | access-date=2024-04-27 }} Studies conducted in the past have also revealed changes in the expression of Bcl-2 and p53 in comparison to benign glomus tumors.{{cite journal | last1=Hegyi | first1=L. | last2=Cormack | first2=G. C. | last3=Grant | first3=J. W. | title=Histochemical investigation into the molecular mechanisms of malignant transformation in a benign glomus tumour | journal=Journal of Clinical Pathology | publisher=BMJ | volume=51 | issue=11 | date=1998-11-01 | issn=0021-9746 | doi=10.1136/jcp.51.11.872 | pages=872–874| pmid=10193335 | pmc=500988 }}

These lesions in soft tissue and skin need to be distinguished from other cutaneous round cell malignancies such hemangiopericytoma, leiomyosarcoma, melanoma, and Merkel cell carcinoma.{{cite journal | last1=Binesh | first1=F. | last2=Akhavan | first2=A. | last3=Zahir | first3=S. T. | last4=Bovanlu | first4=T. R. | title=Clinically malignant atypical glomus tumour | journal=Case Reports | publisher=BMJ | volume=2013 | issue=jan03 1 | date=2013-01-03 | issn=1757-790X | doi=10.1136/bcr-2012-007618 | pages=bcr2012007618| pmid=23291816 | pmc=3603905 }}

Treatment

Although Mohs micrographic surgery has been previously described, the standard of care for malignant glomus tumors still involves wide local excision with negative surgical margins. It is not currently advised to use adjuvant chemotherapy for primary glomangiosarcoma.{{cite journal | last1=Oh | first1=Stephen D. | last2=Stephenson | first2=Daniel | last3=Schnall | first3=Stephen | last4=Fassola | first4=Isabella | last5=Dinh | first5=Paul | title=Malignant Glomus Tumor of the Hand | journal=Applied Immunohistochemistry & Molecular Morphology | publisher=Ovid Technologies (Wolters Kluwer Health) | volume=17 | issue=3 | year=2009 | issn=1541-2016 | doi=10.1097/pai.0b013e31818a9d5d | pages=264–269| pmid=18997618 }}

See also

References

{{Reflist}}

Further reading

  • {{cite journal | last1=Rkiba | first1=Zakaria | last2=Rafai | first2=Mohamed | last3=Rajaallah | first3=Abdessamad | last4=Elkassimi | first4=Charafeddine | last5=Garch | first5=Abdelhak | title=Malignant glomus tumor of the foot. Case report | journal=International Journal of Surgery Case Reports | publisher=Elsevier BV | volume=79 | year=2021 | issn=2210-2612 | doi=10.1016/j.ijscr.2021.01.050 | pages=413–416 | pmid=33524797 | pmc=7851418 | ref=none}}
  • {{cite journal | last1=Abu-Zaid | first1=Ahmed | last2=Azzam | first2=Ayman | last3=Amin | first3=Tarek | last4=Mohammed | first4=Shamayel | title=Malignant Glomus Tumor (Glomangiosarcoma) of Intestinal Ileum: A Rare Case Report | journal=Case Reports in Pathology | publisher=Hindawi Limited | volume=2013 | year=2013 | issn=2090-6781 | doi=10.1155/2013/305321 | doi-access=free | pages=1–5 | pmid=23691399 | pmc=3638502 | ref=none}}