SchookCC, MullikenJB, FishmanSJ, GrantFD, ZurakowskiD, GreeneAK. Primary lymphedema: Clinical features and management in 138 pediatric patients. Plast Reconstr Surg, 2011; 197:2419–2431.
2.
GreeneAK, SchookCC. Primary lymphedema: Definition of onset based on developmental age. Plast Reconstr Surg, 2012; 129:221e–222e.
3.
MaclellanRA, CoutoRA, SullivanSE, GrantFD, SlavinSA, GreeneAK. Management of primary and secondary lymphedema: Analysis of 225 referrals to a center. Ann Plast Surg, 2014, Apr8. [Epub ahead of print].
4.
HassaneinAH, MullikenJB, FishmanSJ, GreeneAK. Evaluation of terminology for vascular anomalies in current literature. Plast Reconstr Surg, 2011; 127:347–351.
5.
StewartFW, TrevesN. Lymphangiosarcoma in postmastectomy lymphedema: A report of six cases in elephantiasis chirurgica. Cancer, 1948; 1:64–81.
6.
JessnerM, ZakFG, ReinCR. Angiosarcoma in postmastectomy lymphedema (Stewart-Treves syndrome). AMA Arch Derm Syphilol, 1952; 65:123–129.
7.
BroströmLA, NilsonneU, KronbergM, SoderbergG. Lymphangiosarcoma in chronic hereditary oedema (Milroy's disease). Ann Chir Gynaecol, 1989:78:320–323.
8.
AnderssonHC, ParryDM, MulvihillJJ. Lymphangiosarcoma in late-onset hereditary lymphedema: Case report and nosological implications. Am J Med Gene, 1995; 56:72–75.
9.
Hallel-HalevyD, YerushalmiJ, GrunwaldMH, AvinoachI, HalevyS. Stewart-Treves syndrome in a patient with elephantiasis. J Am Acad Dermatol, 1999; 41:349–350.
10.
DürrHR, PellengahrC, NerlichA, BaurA, MaierM, JanssonV. Stewart-Treves syndrome as a rare complication of a hereditary lymphedema. Vasa, 2004; 33:42–45.
11.
ShonW, WadaDA, FolpeAL, PittelkowMR. Angiosarcoma in a patient with congenital nonhereditary lymphedema. Cutis 90, 2012; 90:248–251.
SprangerJ, BenirschkeK, HallJG, LenzW, LowryRB, OpitzJM, PinskyL, ScharzacherHG, SmithDW. Errors of morphogenesis: Concepts and terms. Recommendations of an International Working Group. J Pediatr, 1982; 110:160.
16.
CohenMM. Syndromes, Associations, and Sequences. In: CohenMM ed. The Child with Multiple Birth Defects. 2nd ed. New York: Oxford University Press; 1997: pp. 3–5.
Mosby's Medical Dictionary. 8th ed. St. Louis: Elsevier Mosby; 2009: 1442.
19.
EnjolrasO, WassefM, MazoyerE, FriedenIJ, RieuPN, DrouetL, TaiabA, StalderJF, EscandeJP. Infants with kasaback-merritt syndrome do not have “true” hemangiomas. J Pediatr, 1997; 130:631–640.
20.
SarkarM, MullikenJB, KozakewichHP, RobertsonRL, BurrowsPE. Thrombocytopenic coagulopathy (Kasabach Merritt phenomenon) is associated with kaposiform hemangioendothelioma and not with common infantile hemangioma. Plast Reconstr Surg, 1997; 100:1377–1386.
21.
MullikenJB, AnupindiS, EzekowitzRA, MihmMCJr.Case 13-2004: A newborn girl with a large cutaneous lesion, thrombocytopenia, and anemia. New Engl J Med, 2004; 350:1764–1775.