Hemangioma in a pulmonary hilar lymph node: Case report

<p>Abstract</p> <p>Background</p> <p>Different types of vascular proliferation may occur in lymph nodes, but hemangiomas in lymph nodes are extremely rare.</p> <p>Case Presentation</p> <p>A 73-year-old man was found to have a 15-mm nodular shadow in the left lung on computed tomography, and bronchoscopic brush cytology yielded a diagnosis of squamous cell carcinoma. Chest computed tomography showed no evidence of hilar or mediastinal lymphadenopathy. Left lower lobectomy with hilar and mediastinal lymph node dissection was performed. Postoperative histopathological examination revealed squamous cell carcinoma and no lymph node metastasis. On the other hand, a lobar bronchial lymph node presented a small lesion showing the dense proliferation of capillary blood vessels with elastic change. Immunohistochemically, the lesion was positive for factor VIII and CD34, leading to a diagnosis of primary hemangioma of the lymph node.</p> <p>Conclusion</p> <p>To our knowledge, this is the first case reported in the literature of hemangioma in a pulmonary hilar lymph node. Intranodal hemangioma needs to be differentiated from malignant vascular tumors.</p

A lymph nodal capillary-cavernous hemangioma

A capillary-cavernous hemangioma in an obturator lymph node was found incidentally in a 64 year-old woman who had undergone unilateral salpingo- oophorectomy and lymphadenectomy for an ovarian neoplasm. Vascular tumors of lymph nodes are briefly reviewed including eight previously described nodal capillary-cavernous hemangiomas. The association with other splanchnic hemangiomas is pointed out and the likelihood that the lesion is a hamartoma rather than a true neoplasm is addressed. Despite its rarity, this entity needs to be recognized by lymphologists who image lymph nodes by lymphangiography as well as by lymph nodal pathologists

The Lipoleiomyoma of uterus [Il lipoleiomioma dell'utero]

The presence of fatty tissue in the myometrium is anomalous; this alteration has been interpreted either as a lipomatous degeneration or as a metaplasia of smooth muscle cells or, still, as a real neoplasm, frequently associated with a leiomyoma, the so-called lipoleiomyoma. The observation of a case of lipoleiomyoma stimulated us to ascertain the real incidence of this lesion which is commonly considered to be rare. We examined 620 single or multiple uterine leiomyomas with extensive sampling of all the areas suspected to contain fatty tissue islands. Five times out of seven the presence of fat cells in a leiomyoma resulted to be a true lipoleiomyoma. It has thus been possible to ascertain the incidence of lipoleiomyoma versus uterine leiomyomatosis (0,8%). Futhermore we observed a prevalence in menopause, an association with multiple leiomyoma and a preferential onset in the subserosa. The pathogenesis of this lesion, which can be fully ascribed to a mixed, benign, heterologous, mesenchymal neoplasm, is briefly discussed