{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,12]],"date-time":"2026-05-12T20:53:41Z","timestamp":1778619221519,"version":"3.51.4"},"reference-count":11,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2015,7,6]],"date-time":"2015-07-06T00:00:00Z","timestamp":1436140800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatric Blood &amp; Cancer"],"published-print":{"date-parts":[[2015,11]]},"abstract":"<jats:sec><jats:label\/><jats:p>Subcutaneous panniculitis\u2010like T\u2010cell lymphoma (SPTCL) and primary cutaneous gamma delta T\u2010cell lymphoma (PCGD\u2010TCL) were initially both classified as subcutaneous panniculitis\u2010like T\u2010cell lymphoma. In 2008, SPTCL with alpha\u2010beta T\u2010cell receptor subtype was separated from primary cutaneous gamma delta T\u2010cell lymphomas (PCGD\u2010TCL). We report four pediatric cases that demonstrate the heterogeneity of each disease and show that PCGD\u2010TCL in children can have an indolent course, whereas SPTCL can behave aggressively. Three patients had spontaneous, durable remissions without treatment, whereas the one patient with disease progression was treated successfully. Watchful waiting may thus be appropriate for initial management of children. 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