TY - JOUR
T1 - Clear cell 'sugar' tumor of the lung
T2 - Association with lymphangioleiomyomatosis and multifocal micronodular pneumocyte hyperplasia in a patient with tuberous sclerosis
AU - Flieder, Douglas B.
AU - Travis, William D.
PY - 1997
Y1 - 1997
N2 - We report the unique association of a clear cell 'sugar' tumor of the lung (CCTL) in a 32-year-old woman with tuberous sclerosis (TSC), lymphangioleiomyomatosis (LAM), and multifocal micronodular pneumocyte hyperplasia (MMPH). Chest radiographs demonstrated a peripheral solitary 1.0- cm lingular nodule, diffuse emphysematous changes, and bilateral pneumothorax. Microscopic examination of the coin lesion showed an unencapsulated tumor composed of round to oval to locally spindled cells with distinct cellular borders, abundant clear to eosinophilic granular cytoplasm, prominent thin-walled blood channels, and focal hyaline stroma. Rare multinucleated cells were identified, and neither necrosis nor mitotic figures were seen. Tumor cells contained abundant diastase-sensitive intracytoplasmic glycogen, as demonstrated with periodic acid-Schiff stains. Tumor cell immunoreactivity for HMB-45 and nonreactivity for cytokeratin supported the diagnosis. The lung tissue also contained MMPH and smooth muscle proliferations diagnostic of LAM. The histogenesis of CCTL remains controversial, and similarities between this lesion and both LAM and angiomyolipoma (AML) raise the possibility that these lesions are related not only to each other, but that CCTL should be added to the spectrum of pulmonary manifestations of TSC.
AB - We report the unique association of a clear cell 'sugar' tumor of the lung (CCTL) in a 32-year-old woman with tuberous sclerosis (TSC), lymphangioleiomyomatosis (LAM), and multifocal micronodular pneumocyte hyperplasia (MMPH). Chest radiographs demonstrated a peripheral solitary 1.0- cm lingular nodule, diffuse emphysematous changes, and bilateral pneumothorax. Microscopic examination of the coin lesion showed an unencapsulated tumor composed of round to oval to locally spindled cells with distinct cellular borders, abundant clear to eosinophilic granular cytoplasm, prominent thin-walled blood channels, and focal hyaline stroma. Rare multinucleated cells were identified, and neither necrosis nor mitotic figures were seen. Tumor cells contained abundant diastase-sensitive intracytoplasmic glycogen, as demonstrated with periodic acid-Schiff stains. Tumor cell immunoreactivity for HMB-45 and nonreactivity for cytokeratin supported the diagnosis. The lung tissue also contained MMPH and smooth muscle proliferations diagnostic of LAM. The histogenesis of CCTL remains controversial, and similarities between this lesion and both LAM and angiomyolipoma (AML) raise the possibility that these lesions are related not only to each other, but that CCTL should be added to the spectrum of pulmonary manifestations of TSC.
KW - Adenocarcinoma, Clear Cell/chemistry
KW - Adult
KW - Biomarkers, Tumor/analysis
KW - Female
KW - Humans
KW - Hyperplasia/pathology
KW - Immunohistochemistry
KW - Lung Neoplasms/chemistry
KW - Lymphangioleiomyomatosis/pathology
KW - Tuberous Sclerosis/pathology
UR - http://www.scopus.com/inward/record.url?scp=0030864878&partnerID=8YFLogxK
U2 - 10.1097/00000478-199710000-00017
DO - 10.1097/00000478-199710000-00017
M3 - Article
C2 - 9331299
AN - SCOPUS:0030864878
SN - 0147-5185
VL - 21
SP - 1242
EP - 1247
JO - American Journal of Surgical Pathology
JF - American Journal of Surgical Pathology
IS - 10
ER -