Primary Left Ventricular Angiomatosis First Description of a Rare Vascular Tumor in the Left Heart

Kırma, Cevat; Izgi, Akin; Yakut, Cevat; Güler, Mustafa; Can, Mehmet Mustafa; Zemherı, Ebru

doi:10.1536/ihj.47.469

Cited by 12 publications

(13 citation statements)

References 14 publications

(10 reference statements)

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“…A second but uncommon pattern is the clusters of capillary-sized vessels arranged in nodules around a large vessel in the center. Both types are typically associated with large amounts of adipose tissue and hence these lesions have lead previous authors to use the term ‘infiltrating angiolipoma’, suggesting that these are more generalized mesenchymal proliferations rather than exclusive vascular pathology [8]. Similar histopathologic features are seen in the present case reports.…”

Section: Discussionsupporting

confidence: 76%

“…The congenital form may be seen sporadically or accompanying certain types of syndromes such as Klippel–Trenaunay–Weber syndrome, Sneddon’s syndrome, or Gorham disease [8]. The acquired form of angiomatosis may be infectious or iatrogenic.…”

Section: Discussionmentioning

confidence: 99%

“…Bartonellosis and HIV are associated with angiomatosis. Iatrogenic cases occur after AV fistula formation or trauma [8]. …”

Section: Discussionmentioning

confidence: 99%

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Angiomatosis in the Head and Neck—3 Case Reports

Shetty

Prabhu

2009

Head and Neck Pathol

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Angiomatosis is a diffuse vascular lesion which involves a large segment of the body in a contiguous fashion involving multiple tissues (e.g. subcutis, muscle, bone, adipose tissue etc.) in different planes. Such lesions usually present in the first two decades of life with female predilection and are commonly seen in lower extremities. It clinically mimics hemangioma or vascular malformation and its surgical removal is difficult because of its infiltrative nature and thus has high recurrence rate (90%). Therefore a precise histopathological diagnosis of angiomatosis is important to achieve a curative resection. Histopathologically it consists of proliferating blood vessels of varying caliber, infiltrating into the soft tissues. Proliferating capillaries are seen within or adjacent to major vessels. Few cases are reported in head and neck region. This article highlights three unusual cases of angiomatosis reported as benign lesions, in rare sites such as the malar region (predominantly infiltrating the adipose tissue), within the masseter (predominantly infiltrating the muscle) and in the mandible (infiltrating the bone). Histopathological differential diagnosis is also discussed.

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Section: Discussionsupporting

confidence: 76%

Section: Discussionmentioning

confidence: 99%

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Angiomatosis in the Head and Neck—3 Case Reports

Shetty

Prabhu

2009

Head and Neck Pathol

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“…Angiomatosis may be congenital, and is associated with certain types of syndromes such as Klippel‐Trenaunay‐Weber syndrome, Sneddon syndrome, von Hippel‐Lindau, or Gorham disease. There are also infectious forms of angiomatosis associated with Bartonella and human immunodeficiency virus 4…”

Section: Discussionmentioning

confidence: 99%

“…There are also infectious forms of angiomatosis associated with Bartonella and human immunodeficiency virus. 4 Angiomatosis can be confused clinically and radiographically with other vascular lesions, and as such it is the histopathologic diagnosis that reveals the true nature of the disease process. The tendency for recurrence requiring further surgery is >90%, with nearly 40% of patients experiencing more than one recurrence within 5 years.…”

Section: Discussionmentioning

confidence: 99%

Angiomatosis of the paranasal sinuses

et al. 2012

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Angiomatosis is a rare benign lesion of the head and neck that can be mistaken for either a vascular malformation or malignant disease as a result of its infiltrative nature. The recurrence rate of angiomatosis requiring surgery is reported to be >90%, and as such the otolaryngologist treating this condition should endeavor to remove all disease during the first operation while maintaining a high level of suspicion for recurrence during postoperative surveillance. This case represents the first report of angiomatosis involving the nose and/or paranasal sinuses, and extends the differential diagnosis of sinonasal tumors, of which the otolaryngologist must be aware. A description of the surgical care and postoperative surveillance recommendations is detailed in this first reported case of angiomatosis of the paranasal sinuses.

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