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Page 1
Histiocytosis X.
Favara BE, McCarthy RC, Mierau GW. Favara BE, et al. Hum Pathol. 1983 Aug;14(8):663-76. doi: 10.1016/s0046-8177(83)80138-5. Hum Pathol. 1983. PMID: 6347865 Review.
To clarify salient issues pertaining to histiocytosis X--a syndrome that includes Letterer-Siwe disease, Hand-Schuller-Christian disease, and eosinophilic granuloma--the authors review the epidemiologic data and the histologic, morphologic, and clinical bases for diagnosis and …
To clarify salient issues pertaining to histiocytosis X--a syndrome that includes Letterer-Siwe disease, Hand-Schuller-Christian disease, an …
Idiopathic differentiated histiocytosis.
Daneshbod K, Kissane JM. Daneshbod K, et al. Am J Clin Pathol. 1978 Sep;70(3):381-9. doi: 10.1093/ajcp/70.3.381. Am J Clin Pathol. 1978. PMID: 309279
Clinically the patients are older and in good general condition during the course of the disease. Histologically histiocytes in these two groups are cytologically benign, and the whole process is inflammatory rather than neoplastic. Presence of giant cells, eosinophils, an …
Clinically the patients are older and in good general condition during the course of the disease. Histologically histiocytes in these …
Langerhans cell histiocytosis of bone.
Stull MA, Kransdorf MJ, Devaney KO. Stull MA, et al. Radiographics. 1992 Jul;12(4):801-23. doi: 10.1148/radiographics.12.4.1636041. Radiographics. 1992. PMID: 1636041 Review.
The three classic syndromes may have considerable clinical overlap: eosinophilic granuloma, in which the disease is limited to bone in patients usually 5-15 years old; Hand-Schuller-Christian disease, characterized by multifocal bone lesions and extraskeletal involvement of the r …
The three classic syndromes may have considerable clinical overlap: eosinophilic granuloma, in which the disease is limited to bone in patie …
Eosinophilic granuloma of bone.
Slater JM, Swarm OJ. Slater JM, et al. Med Pediatr Oncol. 1980;8(2):151-64. doi: 10.1002/mpo.2950080208. Med Pediatr Oncol. 1980. PMID: 6999317 Review.
The most common symptom is pain, with or without swelling. Multiple sites in a single case are frequent. The clinical course is generally benign, unlike Letterer-Siwe disease or Hand-Schuller-Christian disease. ...
The most common symptom is pain, with or without swelling. Multiple sites in a single case are frequent. The clinical course is gener …
Familial occurrence of Letterer-Siwe disease.
Freundlich E, Amit S, Montag Y, Suprun H, Nevo S. Freundlich E, et al. Arch Dis Child. 1972 Feb;47(251):122-5. doi: 10.1136/adc.47.251.122. Arch Dis Child. 1972. PMID: 5018627 Free PMC article.
Letterer-Siwe disease occurred in 4 infant sibs from two consanguineous families. An identical clinical course and pathological picture was observed in all 4 infants. The occurrence of families with multiple cases supports the hypothesis of genetic causation in Letterer-Si …
Letterer-Siwe disease occurred in 4 infant sibs from two consanguineous families. An identical clinical course and pathological pictu …
Letterer-Siwe disease.
Paul VK, Swaminathan S, Choudhary C, Choudhary VP. Paul VK, et al. Indian J Chest Dis Allied Sci. 1983 Oct-Dec;25(4):299-301. Indian J Chest Dis Allied Sci. 1983. PMID: 6679501 No abstract available.
Specific cutaneous manifestations of internal malignancy.
Kaplan RP. Kaplan RP. Adv Dermatol. 1986;1:3-42. Adv Dermatol. 1986. PMID: 3079247 Review.
Those patients who are immunocompromised secondary to concomitant disease or immunosuppressive therapy are more susceptible to a disseminated fulminant course accompanied by opportunistic infection. In conclusion, although specific signs of internal malignancy are less com …
Those patients who are immunocompromised secondary to concomitant disease or immunosuppressive therapy are more susceptible to a disseminate …
Letterer-Siwe disease in an octogenarian.
Caputo R, Berti E, Monti M, Gasparini G, Bertani E. Caputo R, et al. J Am Acad Dermatol. 1984 Feb;10(2 Pt 1):226-33. doi: 10.1016/s0190-9622(84)70027-2. J Am Acad Dermatol. 1984. PMID: 6546937
30 results