Rapidly involuting congenital hemangioma associated with transient anemia and thrombocytopenia

Andreu-Barasoain, Marta; Naz, Elena; Díaz, Mercedes; López-Estebaranz, J.L.

doi:10.1111/j.1365-4632.2011.05091.x

Cited by 6 publications

(3 citation statements)

References 8 publications

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“…In the literature published as RICH and transient thrombocytopenia, there are only 11 cases described, including the case that we have reported, all of them are summarized in Table 1 . 1 , 3 , 4 , 5 …”

Section: Discussionmentioning

confidence: 99%

Rapidly involuting congenital haemangioma (RICH) associated with transient thrombocytopenia and coagulopathy

Palma,

Gracia-Cazaña,

Ruiz de la Cuesta-Martín

et al. 2024

Anais Brasileiros de Dermatologia

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Section: Discussionmentioning

confidence: 99%

Rapidly involuting congenital haemangioma (RICH) associated with transient thrombocytopenia and coagulopathy

Palma,

Gracia-Cazaña,

Ruiz de la Cuesta-Martín

et al. 2024

Anais Brasileiros de Dermatologia

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“…In reported cases of massive (≥5 cm in diameter) CH combined with multiple serious complications with good outcomes, a combination of conservative therapy, vascular embolization, and surgery was mostly used3–8 (Supplemental Table 1, Supplemental Digital Content 1, http://links.lww.com/SCS/E931).…”

Section: Discussionmentioning

confidence: 99%

Multidisciplinary Treatment of a Giant Maxillofacial Congenital Hemangioma With Multiple Severe Complications

Tian

Zhang

2023

Journal of Craniofacial Surgery

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“…28 RICHs may also be rarely associated with mild thrombocytopenia, hypofibrinogenemia, and anemia, which is distinctly different from Kasabach-Merritt phenomenon (KMP), as it resolves spontaneously within 2 weeks and is not associated with bleeding complications. 29,30 Presenting as an asymptomatic abdominal mass in an infant or found incidentally on imaging, single heman-giomas in the liver involute rapidly like RICHs and rarely cause significant issues. 31,32 NICHs are present at birth, do not regress, and grow proportionately with the child.…”

Section: Congenital Hemangiomasmentioning

confidence: 99%

Advances in the Medical Management of Vascular Anomalies

Ricci

2017

Semin intervent Radiol

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Vascular anomalies comprise a spectrum of diseases that are broadly classified as tumors and malformations. Diagnosis is often challenging, given a wide range of clinical presentations with overlapping signs and symptoms. Accurate diagnosis is critical to determine prognosis and to generate a management plan, which frequently involves multiple subspecialists during different phases of treatment. An updated classification system provides structure and clear, consistent terminology, allowing for improved diagnosis, provider communication, and collaboration. Historically, treatment of vascular anomalies was primarily surgical and medical therapies were limited or ineffective. Recent discoveries of pharmacologic agents effective in treating vascular anomalies have broadened our medical therapeutic options, limiting the need for unnecessary or high-risk procedures and improving patients' quality of life.

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Rapidly involuting congenital hemangioma associated with transient anemia and thrombocytopenia

Cited by 6 publications

References 8 publications

Rapidly involuting congenital haemangioma (RICH) associated with transient thrombocytopenia and coagulopathy

Rapidly involuting congenital haemangioma (RICH) associated with transient thrombocytopenia and coagulopathy

Multidisciplinary Treatment of a Giant Maxillofacial Congenital Hemangioma With Multiple Severe Complications

Advances in the Medical Management of Vascular Anomalies

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