Brief clinical and labortory observation
Splenic consumptive coagulopathy in a patient with disseminated lymphangiomatosis

https://doi.org/10.1016/S0022-3476(77)80706-3Get rights and content

First page preview

First page preview
Click to open first page preview

References (10)

  • KasabachHH et al.

    Capillary hemangioma with extensive purpura

    Am J Dis Child

    (1940)
  • HoldenKR et al.

    Diffuse neonatal hemangiomatosis

    Pediatrics

    (1970)
  • KoblenzerPJ et al.

    Angiomatosis (hamartomatous hem-lymphangiomatosis)

    Pediatrics

    (1961)
  • MorphisLG et al.

    Generalized lymphangioma in infancy with chylothorax

    Pediatrics

    (1970)
  • KornfaltR et al.

    Fibrinolysis in lymphangioma

    Acta Paediatr Scand

    (1973)
There are more references available in the full text version of this article.

Cited by (30)

  • Hemorrhagic shock from post-traumatic rupture of microcystic splenic lymphangioma: A case report and review of the literature

    2020, International Journal of Surgery Case Reports
    Citation Excerpt :

    Complications of SL include rupture with hemorrhage and peritonitis, infection, abscess formation, pleural effusion, lung atelectasis, pneumonia, empyema, intestinal obstruction, diaphragmatic immobility, hypertension, tumor enlargement and a low risk of malignant transformation to lymphangiosarcoma [7,10]. Excessive growth of SL can lead to complications such as consumptive coagulopathy, hypersplenism and portal hypertension [15]. According to literature, in our case unknown microcystic SL represented a risk factor for post-traumatic splenic rupture, so diagnosis was made after detection of a complication.

  • A review of the cysts of the spleen

    2016, Diagnostic Histopathology
    Citation Excerpt :

    The differential diagnosis includes haemangiomas, epithelial splenic cysts (epidermoid, mesothelial) and parasitic cysts. Complications associated with larger lymphangiomas include infection, acute peritonitis secondary to rupture, hypersplenism, consumptive coagulopathy, bleeding and portal hypertension.28 Primary mucinous cystadenocarcinoma of the spleen is exceptionally rare with only a few cases reported in the literature.29,30

  • Retroperitoneal lymphangioma

    2006, Asian Journal of Surgery
  • Lymphangiomatosis of the spleen and 2 accessory spleens

    2002, Surgery
    Citation Excerpt :

    Splenic lymphangiomas may also involve the spleen alone, as in the current case, with various manifestations3: focal lesions of small size, subcapsular rather than intraparenchymal, with no pathologic significance; large cystic lesions that may attain sufficient size to cause significant splenomegaly and left-upper quadrant symptoms; and lymphangiomatosis, as illustrated in the current case, in which the spleen is diffusely replaced by the expanding lymphangiomas, leaving little or no recognizable splenic parenchyma. In lymphangiomatosis, the spleen may be considerably enlarged, as in the current case, causing left-upper-quadrant symptoms and involving risks of complications (bleeding, rupture, consumptive coagulopathy, hypersplenism).4 In these cases, a surgical treatment is required.

  • Cervical and thoracic components of multiorgan lymphangiomatosis managed surgically

    2001, Annals of Thoracic Surgery
    Citation Excerpt :

    Our patient presented with atypical chest pain and progressively worsening dyspnea. Dietz and Stuart [9] described a patient with extensive hygromatous change of the spleen leading to sequestration thrombocytopenia and consumptive coagulopathy. Different diagnostic modalities can provide clues to the possible diagnosis.

View all citing articles on Scopus
View full text