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Case Report
A Case of Subcutaneous Panniculitis-like T Cell Lymphoma in Childhood
Yoon Seok Choi, Kyung Mi Shin, Sung Chul Won, Chuhl Joo Lyu, Chang Hyun Yang, Byung Soo Kim, Moon Kyu Kim
Clin Exp Pediatr. 2002;45(8):1028-1032.   Published online August 15, 2002
Subcutaneous pannicultis-like T cell lymphoma is a rare cutaneous T cell lymphoma. It presents with multiple subcutaneous nodules or plaques involving the extremities or trunk, and with constitutional symptoms that include fever, malaise, fatigue, myalgia, chills and weight loss. Histologically, the lesions of this disease are reminiscent of panniculitis and are composed of a mixture of small and large atypical...
A Case of Poststeroid Panniculitis
Hee Seok Koh, Sha Young Choi, Sung Jin Ha, Oh Kyung Lee
Clin Exp Pediatr. 1992;35(3):411-416.   Published online March 15, 1992
Poststeroid panniculitis occuring after steroid treatment is an extremely rare entity. Multiple subcutaneous, firm, pruritic, tender nodules occur chiefly over the cheeks, arms, and trunk in young children following sudden discontinuation of large dose of steroids. We experiened a case of poststeroid panniculitis in a 2day-old female infant with complaints of multiple subcutaneous nodules on cheeks and neck for 10 days....
A Case of Poststeroid Panniculitis
Moon Sang Park, Mee Kyung Nam, Hae Yong Lee, Baek Keun Lim, Jong Soo Kim, Sun Won Hong
Clin Exp Pediatr. 1992;35(3):406-410.   Published online March 15, 1992
Poststeroid panniculitis occuring after steroid treatment is an extremely rare entity. Multiple subcutaneous, firm, pruritic, tender nodules occur chiefly over the cheeks, arms, and trunk in young children following sudden discontinuation of large dose of steroids. We experiened a case of poststeroid panniculitis in a 2day-old female infant with complaints of multiple subcutaneous nodules on cheeks and neck...
Original Article
A case of Weber-Christian disease.
Doo Kweon Kim, Sang Jo Park, Tae Gyu Whang, Soon Yong Lee
Clin Exp Pediatr. 1991;34(8):1157-1162.   Published online August 31, 1991
Weber-Christian disease is a relapsing febrile nodular nonsuppurative inflammation of the subcuta- neous fat tissue. We experianced a case of Weber-Christian disease. The patient was a 10-year-old girl with the complaints of fever, malaise and erythematous painful nodules on extremities, trunk and back. The diagnosis was based on the clinical pictures and the histologic findings. Oral prednisolone therapy was tried and the response occurred...
A Case of Cytophagic Histiocytic Panniculitis.
Hyung Keun Nam, Byong Rai Cho, Don Hee Ahn, Keun Chan Sohn, Jin Hee Sohn
Clin Exp Pediatr. 1989;32(7):995-1000.   Published online July 31, 1989
Cytophagic histiocytic panniculitis is a chronic, benign, visceral and cutaneous histiocytic (cyto- phagic) paniculitis, progressing to liver dysfunction, jaundice and a terminal hemorrhagic diathesis. We have experienced a case of cytophagic histiocytic panniculitis in an 11 year old male who had developed recurrent fever and subcutaneous nooules since infancy, progressing to liver dysfunction, jaundice and hemorrhagic diathesis. The noaular biopsy also showed a characteristic...