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Zacharia, T.T., Ittoop, A., Perumpillichira, J.J. and Chavhan, G. (2003) Sonographic appearance of a congenital parotid gland hemangiolymphangioma simulating malignancy in an infant. Journal of Clinical Ultrasound, 31, 493-496. http://dx.doi.org/10.1002/jcu.10205

has been cited by the following article:

• TITLE: Chronic thromboembolic pulmonary hypertension related to hemangiolymphangioma

  AUTHORS: Tsuneyuki Nakamura, Keita Tamanuki, Giyo Ko, Masato Oguri, Chisato Akita, Chika Kitaoka, Toshimi Nakamura, Yutaka Saikawa

  KEYWORDS: Hemangiolymphangioma; Chronic Thromboembolic Pulmonary Hypertension; Long-Term Follow-Up

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.3 No.1, January 21, 2014

  ABSTRACT: Hemangiolymphangioma (HL) is a congenital anomaly and histologically benign tumor, which was composed of both the lymphatic and the blood vessels. We report an adult case of HL complicated by chronic thromboembolic pulmonary hypertension (CTEPH) in a 20-year-old female. Gastrointestinal bleeding scintigraphy and operative findings elucidate a close relationship between CTEPH and residual HL. This case indicates that HL survivors with remaining left-to-right shunt might lead to CTEPH during the long-term follow-up.