CASE REPORT

A previously healthy 24-year-old woman presented with a headache of two days duration. She was referred to the emergency room of our hospital because she had a history of slip-down in a bathroom two days previously. Precontrast brain computed tomography (CT) revealed a small amount of extra-axial hemorrhage at the right frontotemporal region (Fig. 1A). Skull magnetic resonance images showed a slightly rim-enhancing lesion invading right sphenoid bone. Differential diagnoses included vascular pathologies such as hemangioma and other tumorous conditions. The skull tumor was removed using a navigation system and cranioplasty of the right frontotemporal area was performed using bone cement. Inferolateral temporal dura over the lesion had been focally disrupted, but no gross leakage was observed. After exposing the right temporal fascia and muscle, the lateral wall of the right orbit, zygoma, and a thinned portion of the bone at the pterygoid process were drilled. Removal of the hematoma exposed a multiseptated cystic cavity (Fig. 1B).

Intraoperative frozen biopsy was performed on the cystic portion of right sphenoid bone, and subsequent intraoperative squash cytology revealed moderate cellular smears composed of sheets or clusters of epithelioid cells in an inflammatory cell– rich background (Fig. 2A–D). Histologically, singly scattered or clusters of round-to-elongated tumor cells were found in sclerotic bone (Fig. 2E). Tumor cells with indistinct cell borders were observed in clusters forming meningothelial whorls and had centrally-placed small round and bland nuclei with or without nucleoli. Prominent hemorrhage was present. Individual tumor cells showed abundant eosinophilic cytoplasm with an occasional vacuolated appearance and cytoplasmic clearing resembling oligodendroglioma (Fig. 2F). Neutrophils were abundant (Fig. 2G, left). There was marked perivascular hyalinization and stromal sclerosis (Fig. 2G, right). Mitotic counts were up to 1 per 10 high power fields, necrosis was absent, and occasional atypia was observed. Tumor cells invaded the thick dura mater. They were positive for CD56 (1:100, CD564, Novocastra, Newcastle upon Tyne, UK), CD99 (prediluted, 12E7, Dako, Glostrup, Denmark), INI-1 (1:200, 25/BAF47, BD Bioscience, San Diego, CA, USA), vimentin (1:100, V9, Dako) (Fig. 2H, left), and progesterone receptor (1:200, 16, Novocastra). Tumor cells also displayed focally membranous positivity for epithelial membrane antigen (1:100, E29, Dako) (Fig. 2H, right). However, they were negative for glial fibrillary acidic protein (prediluted, Dako), S-100 protein (polyclonal, 1:600, Dako), smooth muscle actin (1:100, 1A4, Dako), synaptophysin (prediluted, DAK-SYNAP, Dako), chromogranin (1:100, DAK-A3, Dako), CD34 (1:100, QBEnd10, Dako), L1 cell adhesion molecule (1:200, polyclonal, Abcam, Cambridge, UK), OLIG2 (EP112; 1:500, Cell Marque, Rocklin, CA, USA), and STAT6 (S-20, sc-621, 1:150, Santa Cruz Biotechnology, Santa Cruz, CA, USA). The Ki-67 (MIB-1, 1:100, Dako) proliferation index was 3%. Intervening sclerosis stained with periodic acid-Schiff and Masson-trichrome.

Based on the above histology, notably, the clear cell morphology containing one mitosis, meningothelial whorls, and the lack of hypercellularity, macronuclei, small cell formation, or brain invasion, the tumor was determined to be an intraosseous meningioma of the microcystic and meningotheliomatous type (World Health Organization grade I). We diagnosed this case as intraosseous meningioma with dural involvement because the tumor was largely located within the sphenoid bone.

At 5 months of follow-up, the patient was healthy, asymptomatic, and scheduled for annual postoperative follow-ups.

DISCUSSION

Intraosseous occurrence of meningioma, especially in the skull, is uncommon [7]. Plausibly, this rare primary intraosseous meningioma may arise due to aberrant differentiation or localization of pluripotent embryonal precursor cells of the bone, or from misplaced or trapped arachnoid cells along the suture line during molding of the head at birth and after differentiation into meningocytes or arachnoid cap cells [1]. Alternatively, it may arise from arachnoidal cells of blood vessels or nerves traversing the skull [8].

Intraosseous meningioma of the skull can be confused with primary calvarial bone tumors. On CT images, intraosseous meningiomas appear as osteoblastic, osteolytic, or mixed patterns [3,9]. Skull lesions showing osteolytic lesions, as in our case, include epidermoid tumor, multiple myeloma, Langerhans cell histiocytosis, fibrous dysplasia, giant-cell tumor, Paget’s disease, solitary fibrous tumor/hemangiopericytoma (SFT/HPC), hemangioma, osteosarcoma, and ABC [10]. In the present case, the lesion was located in the sphenoid bone and its preoperative radiologic and gross differential diagnoses included ABC, chordoma, chondrosarcoma, and vascular neoplasm [11]. ABC presenting as a locally destructive osteolytic lesion frequently involves the long bones of knee joints and vertebrae and is usually encountered in the first or second decades of life. When ABC occurs in the skull, it is usually located in the skull vault and only rarely in the skull base [11]. The preoperative diagnosis of an intraosseous lytic lesion like meningioma is challenging. The presence of an osteolytic extracranial soft tissue lesion usually raises the suspicion of malignancy [9]. Radiologic differential diagnosis of osteolytic intraosseous meningiomas of the skull should exclude other lytic lesions such as lytic metastasis, multiple myeloma, eosinophilic granuloma, fibrous dysplasia, Langerhans cell histiocytosis, giant-cell tumor, SFT/HPC, and hemangioma. Radiologically, intraosseous meningiomas present osteoblastic findings in about two-thirds of cases, an osteolytic pattern, in around a third, and a mixed osteoblastic-lytic lesion in only 6% of cases [2,9].

Evaluations of skull lesions by fine-needle aspiration are controversial. Cytologic findings of meningioma are diverse and heterogeneous [12], and notable features for differential diagnosis are as follows; cohesive syncytial meningothelial whorls, individual tumor cells showing nuclear inclusions or grooves and wispy collagenous, rather than fibrillary, cytoplasm with occasional short broad cell processes [13]. Tumor cells with indistinct cell borders and subsequent syncytial whorls are the most common. In meningothelial and microcystic type meningiomas, as in the present case, background collagenous sclerosis is observed in tumor cells with vacuolated cytoplasm mixed with scattered inflammatory cells [13]. Although the biologic roles of circulating neutrophils and intratumoral neutrophils in meningiomas remain unclear, the presence of many inflammatory cells including lymphocytes, plasma cells, natural killer cells, and macrophages is common [14]. A high concordance between frozen and permanent diagnoses (up to 99%) has been reported for meningeal tumors [12]. However, frozen cytologic diagnosis in the described case was difficult due to the presence of massive numbers of inflammatory cells, marked hemorrhage, and an unusual location. Scattered stellate, vacuolated cells, and foam cells may be found in regions of microcystic meningiomas [13]. Singly-scattered tumor cells with intracytoplasmic vacuoles in foci of microcystic meningioma resembling atypical chondrocytes of chondrosarcoma and lipoblasts of liposarcoma were occasionally found [15]. Cytologic findings of chondrosarcoma are moderately cellular with clusters of polygonal cells showing occasional binucleation and well-defined cytoplasm with rounded nuclei showing moderate nuclear pleomorphism embedded in a chondromyxoid background, suggestive of chondrosarcoma [15]. Cytologic findings of chordoma are characterized by mucoid and gelatinous fibromyxoid cellular smears and cords or clusters of round epithelioid cells with small round nuclei and scant basophilic cytoplasm and occasional large physaliphorous cells with central small round nuclei and bubbly cytoplasm [16]. Well differentiated chondrosarcoma arising in the sphenoid bone is another entity necessitating differential diagnosis; the findings of bland nuclei and refractile cytoplasmic processes and a lack of chondromyxoid matrix are useful diagnostic features of meningioma [12].

The most important macroscopic frozen differential diagnosis in the described case was ABC. Cytologic findings of ABC are dominated by blood; dispersed fibroblast-like histiocytes with occasional hemosiderin and multinucleated osteoclast-type giant cells containing fragments of collagen [17]. Osteoid and chondroid matrix material as well as woven bone may be present within aspirated or touch smears. Small fragments of bone may also be found. In hemorrhagic cases, as in our case, markedly vascular hemorrhagic SFT/HPC should be distinguished from meningioma. Cytologic findings of SFT/HPC are nonspecific and “patternless”, i.e., heterogeneous, although naked stripped nuclei and scattered ropy collagen fragments are observed in an occasional pseudoalveolar pattern in a hemorrhagic bloody background [18]. The histologic diagnosis of intraosseous meningioma is not as difficult as that based on frozen cytology. One of the important histologic differential diagnoses of meningioma is SFT/HPC. Immunopositivity for both CD34 and STAT6 in SFT/HPC differentiate it from meningioma [19]. At a glance, clear cells mimicking oligodendroglial cells suggest oligodendroglioma [20]. However, oligodendroglioma and meningioma can be differentiated based on the presence of whorls and immunonegativity for OLIG2 in the meningioma. Histologically, ABC features fibroblastic proliferation and scattered giant cells with osteoid and blood-filled spaces lined by giant cells and hemosiderin laden macrophages [17].

Awareness of intraosseous cystic meningioma involving the skull may facilitate the intraoperative diagnosis of this rare condition. The present case cautions that the possibility of intraosseous meningioma should be kept in mind when is it is encountered in an unusual location.

Fig. 1.

(A) Brain magnetic resonance image shows a slightly enhanced lesion (arrow) at the right sphenoid bone. (B) Intraoperative gross examination of the lesion shows cystic spaces filled with blood and solid texture.

Fig. 2.

(A–D) Frozen cytology. (A) The cystic portion of the right sphenoid bone shows singly scattered eosinophilic round to elongated cells with occasional nuclear hyperchromasia. Inset shows thick refractile collagenous cytoplasm with nuclear hyperchromasia. (B) Moderately cellular smears shows sheets of epithelioid cells in a bloody and inflammatory cell–rich background. Inset shows intermixed inflammatory cells in meningothelial whorls. (C) Cellular sheets of round-shaped epithelioid cells with moderate amounts of eosinophilic granular cytoplasm and euchromatic round nuclei, just apposed to the capillary (left). High magnification shows indistinct cell borders (right). (D) High power view shows occasional nuclear inclusions (arrows). (E–H) Histology. (E) Low power view shows sheets of spindle to round-shaped tumor cells, filling the bone. Note the lamellated bone and osteoblastic rimming. (F) Nests of meningothelial cells form microcystic cobweb-like arrangement. Note the microcystic and bubbly cytoplasm. (G) Sheets of spindle-shaped tumor cells are intermixed with inflammatory cells (left). Note the perivascular sclerosis (right). (H) The tumor cells are immunoreactive for vimentin (left) and epithelial membrane antigen (right).

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Figure & Data

References

Citations

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