Xanthogranuloma of the sellar region: a clinicopathological entity different from adamantinomatous craniopharyngioma

被引:85
作者
Paulus, W
Honegger, J
Keyvani, K
Fahlbusch, R
机构
[1] WWU Munster, Inst Neuropathol, D-48129 Munster, Germany
[2] Univ Erlangen Nurnberg, Dept Neuropathol, D-8520 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Dept Neurosurg, D-8520 Erlangen, Germany
关键词
adenohypophysis; cholesterol granuloma; craniopharyngioma; sellar lesions; pituitary;
D O I
10.1007/s004010051001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Xanthogranulomatous change of craniopharyngioma, consisting of cholesterol clefts, macrophages, chronic inflammatory infiltrates, necrotic debris and hemosiderin deposits, has been traditionally considered a hallmark of the adamantinomatous variant, even in the absence of epithelium. Based on a series of 110 craniopharyngioma patients undergoing primary surgery, we found 37 specimens with a predominating xanthogranulomatous component. Only 3 of these cases (8%) exhibited additional histological features of adamantinomatous craniopharyngioma, while 13 cases (35%) contained non-adamantinomatous epithelium composed of squamous or ciliated cuboidal cells. Subsequent clinical analysis revealed that these 37 xanthogranulomatous lesions differed from 59 classical adamantinomatous craniopharyngiomas with respect to preferential occurrence in adolescents and young adults (mean age 27 years), predominant intrasellar location, smaller tumor size, more severe endocrinological deficits, longer preoperative history, lower frequency of calcification and visual disturbances, better resectability, and a more favorable outcome. On the other hand, xanthogranulomatous and adamantinomatous lesions did not differ with respect to sex, amount of cystic components, or the intraoperative aspect, considered by the neurosurgeon as being typical for craniopharyngioma in all cases. We suggest that xanthogranuloma (cholesterol granuloma) of the sellar region is clinically and pathologically distinct from the classical adamantinomatous craniopharyngioma.
引用
收藏
页码:377 / 382
页数:6
相关论文
共 20 条
  • [1] CORRELATION OF CLINICAL AND PATHOLOGICAL FEATURES IN SURGICALLY TREATED CRANIOPHARYNGIOMAS
    ADAMSON, TE
    WIESTLER, OD
    KLEIHUES, P
    YASARGIL, MG
    [J]. JOURNAL OF NEUROSURGERY, 1990, 73 (01) : 12 - 17
  • [2] Burger PC., 1991, Surgical pathology of the nervous system and its coverings, V3rd edn, P537
  • [4] PAPILLARY CRANIOPHARYNGIOMA - A CLINICOPATHOLOGICAL STUDY OF 48 CASES
    CROTTY, TB
    SCHEITHAUER, BW
    YOUNG, WF
    DAVIS, DH
    SHAW, EG
    MILLER, GM
    BURGER, PC
    [J]. JOURNAL OF NEUROSURGERY, 1995, 83 (02) : 206 - 214
  • [5] Petrous apex cholesterol granulomas: Evolution and management
    Eisenberg, MB
    Haddad, G
    AlMefty, O
    [J]. JOURNAL OF NEUROSURGERY, 1997, 86 (05) : 822 - 829
  • [6] SUPRASELLAR PAPILLARY SQUAMOUS EPITHELIOMA (PAPILLARY CRANIOPHARYNGIOMA)
    GIANGASPERO, F
    BURGER, PC
    OSBORNE, DR
    STEIN, RB
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1984, 8 (01) : 57 - 64
  • [7] XANTHOGRANULOMATOUS COLLOID CYST OF THE 3RD VENTRICLE
    HADFIELD, MG
    GHATAK, NR
    WANGER, GP
    [J]. ACTA NEUROPATHOLOGICA, 1985, 66 (04) : 343 - 346
  • [8] TRANSSPHENOIDAL MICROSURGERY FOR CRANIOPHARYNGIOMA
    HONEGGER, J
    BUCHFELDER, M
    FAHLBUSCH, R
    DAUBLER, B
    DORR, HG
    [J]. SURGICAL NEUROLOGY, 1992, 37 (03): : 189 - 196
  • [9] JANZER RC, 1997, PATHOLOGY GENETICS T, P196
  • [10] Kleihues P., 1993, HISTOLOGICAL TYPING