Literature DB >> 16220316

[Hemangiopericytoma (extrapleural solitary fibrous tumour). Exemplified and discussed on the basis of two cases].

F Wilde1, M Neid, T Schulz, I Sterker, A Hemprich, B Frerich.   

Abstract

BACKGROUND: Hemangiopericytoma was first mentioned in 1942. It is a very uncommon potentially malignant vascular tumour which can occur at every site of the body. According to the WHO, most of the tumours formerly diagnosed as hemangiopericytomas are considered to be extrapleural solitary fibrous tumours. The diagnosis of "hemangiopericytoma" is now only determined if a constant histological picture of hemangiopericytoma is present. The tumour can lead to lymphogenous or hematogenous metastasis. The major location of occurrence is the cutis and subcutis. It originates from the pericytes of the vascular wall. This is reflected in its vascular character and therefore the hemangiopericytoma might clinically be mistaken for a hemangioma. CASE REPORTS: Patient 1: 60 years, female; diagnosis: malignant suboccipital hemangiopericytoma; size: 4.9 x 4.5 x 4.2 cm; pT1bNXMX L0 V0 Pn0; stage IA; grading G1; R0.Patient 2: 38 years, male; diagnosis: benign hemangiopericytoma infraorbital left; size 1.5 x 1.5 x 1.5 cm. DISCUSSION: Most often the hemangiopericytoma becomes clinically conspicuous as a slowly growing, painless swelling. The consistency ranges from soft to dense, and the color is greyish-blue. The slow and painless growth carries the danger of a clinically wrong diagnosis and thus delayed therapy. The histological diagnosis of hemangiopericytoma is determined by biopsy. Besides histology, MRI and angiography are methods that can be employed to diagnose hemangiopericytoma. The therapy of choice is the complete tumour-resection with a safety margin of 1 cm. In the case of an aggressive growth pattern, adjuvant postoperative radiotherapy is recommended. Until now there has been no documented specific therapy concept for managing incomplete resection and the occurrence of metastasis. There are reports about chemo- and radiotherapy either on their own or combined which evidence differing degrees of success. Lifelong monitoring is necessary because recrudescences and metastases can occur even decades later.

Entities:  

Mesh:

Year:  2005        PMID: 16220316     DOI: 10.1007/s10006-005-0649-x

Source DB:  PubMed          Journal:  Mund Kiefer Gesichtschir        ISSN: 1432-9417


  21 in total

1.  Malignant hemangiopericytoma of the bone.

Authors:  H R Dürr; A Nerlich; A Lienemann; P E Müller; H J Refior
Journal:  Langenbecks Arch Surg       Date:  2000-04       Impact factor: 3.445

2.  Tumors featuring pericytes; glomus tumor and hemangiopericytoma.

Authors:  A P STOUT
Journal:  Lab Invest       Date:  1956 Mar-Apr       Impact factor: 5.662

3.  Current management and clinical outcome of hemangiopericytomas.

Authors:  J P Craven; T M Quigley; J W Bolen; E J Raker
Journal:  Am J Surg       Date:  1992-05       Impact factor: 2.565

4.  Malignant hemangiopericytoma in three kindred members of one family.

Authors:  J T Plukker; H S Koops; I Molenaar; A Vermey; L P ten Kate; J Oldhoff
Journal:  Cancer       Date:  1988-02-15       Impact factor: 6.860

5.  [Morphology and clinical signs of hemangiopericytoma. An analysis of 84 cases with a personal contribution].

Authors:  H Neumann
Journal:  Pathologe       Date:  1983-03       Impact factor: 1.011

6.  [Clinical aspects and therapy of hemangiopericytoma].

Authors:  F Ghussen; K Nagel
Journal:  Schweiz Med Wochenschr       Date:  1981-03-14

7.  Hemangiopericytoma of the head and neck.

Authors:  J F Carew; B Singh; D H Kraus
Journal:  Laryngoscope       Date:  1999-09       Impact factor: 3.325

8.  Radiosensitive hemangiopericytoma of the falx. Case report.

Authors:  M Takase; O Watanabe
Journal:  J Neurosurg       Date:  1988-04       Impact factor: 5.115

9.  Hemangiopericytoma. An analysis of 106 cases.

Authors:  F M Enzinger; B H Smith
Journal:  Hum Pathol       Date:  1976-01       Impact factor: 3.466

10.  The pathology of head and neck tumors: vasoformative tumors, part 9B.

Authors:  J G Batsakis; D H Rice
Journal:  Head Neck Surg       Date:  1981 Mar-Apr
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