Detailed analysis of a superficial CD34‑positive fibroblastic tumor: A case report and review of the literature

Introduction

Superficial cluster of differentiation (CD)34-positive fibroblastic tumors (SCPFTs), first identified by Carter et al (1) are rare mesenchymal neoplasms of intermediate (borderline) malignancy. As they were only described recently, their characteristics are yet to be entirely elucidated. They were cured by surgery and had a good outcome (1). Previous studies of SCPFTs have lacked imaging data or cytogenetic analyses of this tumor type (1–4).

The present study describes a patient with SCPFT located in the subcutaneous adipose tissue of the thigh of an 18-year-old man. The imaging, histopathological and ultrastructural data, and the cytogenetic study results are discussed. Aside from histopathology and immunohistochemistry, the examination of this patient encompassed computed tomography (CT), magnetic resonance imaging (MRI), and positron emission tomography (PET)-CT, and cytogenetic analysis to identify chromosomal aberrations. Informed consent for publication of these data was obtained from the patient.

Case report

Clinical and imaging data

An 18-year-old Japanese male noticed a painless mass measuring ~3 cm in the medial aspect of his right distal thigh, without history of trauma. He visited Matsue City Hospital (Matsue, Japan) in April, 2015, where the mass was initially diagnosed as an epidermoid cyst. Surgical resection of the mass was planned, but was cancelled subsequent to the patient developing a cold. The patient was subsequently lost to follow-up for 18 months, following which he revisited Matsue City Hospital as the mass had continued to grow. At that point, a soft tissue sarcoma was suspected. He was referred to Tottori University Hospital (Yonago, Japan) in October, 2016 for evaluation and treatment. Physical examination revealed a 9-cm, hard, elastic mass in his distal thigh without tenderness or warm sensation, but with varicosis (Fig. 1). Medical and family history were unremarkable. The white blood cell count (3.8–8.8×103/µl) and the levels of C-reactive protein (<0.15 mg/dl), alkaline phosphatase (106–322 U/l) and lactate dehydrogenase (124–222 U/l) were normal. CT revealed a well-marginated tumor without calcification in the subcutaneous adipose tissue, and enhanced CT revealed weak enhancement within the lesion (Fig. 2A and B). The tumor demonstrated abnormal uptake on 2-(18F) fluoro-2-deoxy-D-glucose (18F-FDG) PET, with a maximum standardized uptake value of 2.57 (Fig. 2C). The MRI scan revealed a clearly defined tumor measuring 87×70×80 mm and located in the subcutaneous adipose tissue; however, part of the tumor margin appeared to slightly infiltrate the subcutaneous adipose tissue (Fig. 3). Although the tumor appeared to be in close proximity to the vastus medialis and sartorius muscles, it did not infiltrate them. The tumor exhibited homogenous low signal intensity on T1-weighted imaging (Fig. 3A) and high signal intensity on T2-weighted imaging, with small lobulated structures (Fig. 3B). Mild enhancement was observed throughout the tumor, while strong enhancement was evident at the periphery of the small lobulated structures (Fig. 3C). No distant or lymph node metastasis was observed.

Figure 1. Physical examination revealed a 9-cm, hard, elastic mass in the distal thigh of the patient without tenderness or warm sensation, but with varicosis. (A) Frontal view. (B) Medial view.

Figure 2. (A) Plain CT revealed that the tumor was located in the subcutaneous adipose tissue, and was well-circumscribed. (B) Enhanced CT revealed diffuse and weak enhancement in the tumor. (C) The maximum standardized update value of the tumor was 2.57 on positron emission tomography-CT. CT, computed tomography.

Figure 3. Representative horizontal magnetic resonance images. The tumor was located in the subcutaneous adipose tissue, close to the vastus medialis and sartorius muscles, and exhibited a relatively well-defined margin. (A) T1-weighted imaging demonstrated low signal intensity in the mass. (B) T2-weighted imaging revealed high signal intensity, with small lobulated structures. (C) Mild enhancement was observed throughout the tumor, and strong enhancement was observed at the periphery of the small lobulated structures.

Based on the aforementioned clinical data and imaging examinations, the mass was diagnosed as a malignant tumor of the soft tissue; such tumors include synovial sarcoma, alveolar soft part sarcoma, and epithelioid sarcoma. Core needle biopsy was performed for histopathological diagnosis. Although the tumor was suspected to be an SCPFT, a definite diagnosis was not initially available. The differential diagnosis was pleomorphic sarcoma. Thereafter, wide resection was performed.

Pathological data (surgical specimen)

Grossly, the tumor was well-circumscribed and confined to the superficial fibroadipose tissues. It exhibited a yellow and fleshy appearance with small lobulated structures (Fig. 4).

Figure 4. Cut section of tumor. The tumor was well-circumscribed and had a yellow, fleshy appearance with small lobulated structures.

For light microscopic examination (magnification ×100 to ×400), the tumor was fixed in 10% buffered-formalin for 24 h at room temperature, and embedded in paraffin wax. Serial sections, 4 µm thick, were stained using hematoxylin (Mayer's hematoxylin solution) and 0.5% eosin. Histopathologically, the tumor was well-circumscribed and had not infiltrated into adjacent tissues. It was composed of irregular spindle-to-oval-shaped cells, with eosinophilic glassy cytoplasm and hyperchromatic, bizarre and pleomorphic nuclei that frequently demonstrated intranuclear pseudoinclusions. Tumor cells were arranged in fascicles and sheets, with a focal myxoid change in the background. A small number of inflammatory cells, predominantly lymphocytes, were identified throughout the lesion. Mitotic figures were rarely observed (2/50 high-powered fields), and atypical mitoses were not observed (Fig. 5A-F). No necrosis was observed.

Figure 5. Histological and immunohistochemical staining of the tumor. Staining methods included (A-F) hematoxylin and eosin, and antibodies against (G) CD34 and (H) MIB-1. (A) The lesion was well-circumscribed and had not invaded the subcutaneous tissue. (B-F) The tumor was composed of fascicles or sheets of pleomorphic spindle-to-oval-shaped cells that exhibited irregularly hyperchromatic, bizarre and pleomorphic nuclei with frequent intranuclear pseudoinclusions and rare mitotic figures. (C) A small number of inflammatory cells were identified throughout the lesion. (D) Partial myxoid stroma was observed. (G) Immunohistochemically, CD34 was strongly and diffusely expressed in almost all of the tumor cells. (H) The MIB-1 labeling index was 8.6%. Scale bars: (A) 200 µm; (B and C) 100 µm; (D-H) 20 µm. CD, cluster of differentiation; MIB-1, Mindbomb E3 ubiquitin protein ligase 1.

For immunohistochemical analysis, paraffin-embedded tumor tissue specimens were cut into 4-µm sections, then dewaxed in xylene, rehydrated through a graded series of ethanol solutions and rinsed in distilled water for 5 min. Endogenous peroxidase activity was blocked by 2% hydrogen peroxide in methanol at room temperature for 30 min. Subsequent to rinsing with PBS, the sections were incubated with blocking serum (2% fetal bovine serum) at room temperature for 20 min and incubated at 4°C overnight with each primary antibody. Immunohistochemically (by light microscope with magnification, ×100 to ×200), the tumor cells were diffuse and strongly positive for CD34 (catalog no. 413111, prediluted, ready to use; Nichirei, Tokyo, Japan; Fig. 5G) and negative for CD31 (catalog no. M0823, prediluted, ready to use; Dako; Agilent Technologies, Inc., Santa Clara, CA, USA), desmin (catalog no. 413651, prediluted, ready to use; Nichirei Bioscience, Tokyo, Japan), α-smooth muscle actin (catalog no. M0851, dilution, 1:100; Dako; Agilent Technologies, Inc.), S-100 protein (catalog no. 422091, prediluted, ready to use; Nichirei Bioscience), cytokeratin (AE1/AE3; catalog no. 412811, prediluted, ready to use; Nichirei Bioscience), epithelial membrane antigen (catalog no. M0613, prediluted, ready to use; Dako; Agilent Technologies, Inc.), signal transducer and activator of transcription 6 (STAT6; catalog no. sc-29497, dilution, 1:300; Santa Cruz Biotechnology, Inc., Dallas, TX, USA), B-cell lymphoma-2 (catalog no. 413141, prediluted, ready to use; Nichirei Bioscience) and c-Kit (catalog no. A4502, dilution 1:100; Dako; Agilent Technologies, Inc.). Integrase interactor 1 protein (INI1; catalog no. A301-087A dilution, 1:250; Bethyl Laboratories, Montgomery, TX, USA) was expressed throughout the lesion. The Mindbomb E3 ubiquitin protein ligase 1 (MIB1; catalog no. M7240, dilution, 1:100; Dako; Agilent Technologies, Inc.) labeling index in the tumor was 8.6% (Fig. 5H).

Ultrastructural examination

For transmission electron microscopic study, the tumor was fixed overnight at 4°C in 2.5% glutaraldehyde in 0.1 M cacodylate buffer, pH 7.4, followed by post-fixation for 1–2 h in 0.1 M cacodylate-buffered 1% osmium tetraoxide. Subsequent to dehydration in a series of graded ethanol and n-butyl glycidyl ether solutions, cells were embedded in epoxy resin and allowed to set for 48 h at 60°C. Ultrathin sections were stained with uranyl acetate and lead citrate, and examined with an electron microscope. The tumor consisted of spindle-to-oval shaped cells without intercellular junctions. The cells had irregular or convoluted nuclei with abundant, euchromatin-prominent nucleoli. The cytoplasmic organelles consisted of scattered, abundant and rough endoplasmic reticulum, mitochondria, lysosomes, ribosomal rosettes and aggregated lipid globules (Fig. 6).

Figure 6. Transmission electron microscopy. Ultrastructural examination revealed that the tumor cells possessed irregular or convoluted nuclei with abundant euchromatin-prominent nucleoli. In the cytoplasm, aggregated lipid globules were observed. Scale bar, 5 µm.

Cytogenetic studies

Cytogenetic analysis was performed on the surgical specimen. The tissues were cut into pieces and transferred to culture solution. Cell culture and G-band karyotyping were performed by SRL Inc. (Tokyo, Japan). Of the 18 metaphase cells available for analysis, 14 were of normal (46,XY) karyotype, 2 cells had a karyotype of t(2;5)(q31;q31), 1 had a karyotype of 42,Y,-X,-10,-18,-19, add(19)(p13), and 1 had a karyotype of t(7;14)(q21;q24) (Fig. 7).

Figure 7. Tumor cell chromosomes exhibit a translocation between chromosomes 2 and 5 (arrows).

The tumor was finally diagnosed definitively as an SCPFT of the thigh based on clinical, histological and immunohistochemical data. In particular, the results that CD34 was strongly positive on immunohistochemistry, and that the tumor site was superficial, assisted with the diagnosis. The postoperative course (5 months subsequent to surgery) has been uneventful, with no evidence of recurrence or metastasis.

Discussion

When this tumor type was first described in 2014 in a series of 18 cases, Carter et al (1) proposed the descriptive term SCPFT based on clinical, morphological and immunochemical data. To date, only five case series of SCPFT have been described (1–5), in which almost all tumors were described histopathologically and immunohistochemically. Only one study, that of Li et al (5), described imaging data, namely T1-weighted MRI findings. To the best of our knowledge, CT and PET-CT features of SCPFT have not been described prior to the present study.

The available studies on SCPFT described certain shared characteristics: A fibroblastic tumor of the superficial soft tissues with cellular pleomorphism, an extremely low mitotic rate, and strong diffuse CD34 positivity (1–5). In their 18-case series, Carter et al (1) described SCPFTs as slow-growing masses that are present for at least 1 year prior to diagnosis, that range in size from 1.5 to 10 cm (mean, 4.1 cm), and that most commonly afflict adults (age range, 20–76 years; median, 38 years) of any sex (10 males and 8 females). In two-thirds of the cases, the tumors occurred in the lower limbs, including the thighs. All of the tumors showed confinement to the superficial fibroadipose tissues, and absent or minimal involvement of the subjacent muscle was observed. There was no history of a previous cutaneous neoplasm at the same location in any of the patients. Clinical follow-up data (median duration, 24 months; range, 1–104 months) were available for 13 of the 18 patients (72%). Of these 13 patients, 12 were alive with no evidence of disease when the study was published, and 1 patient with a tumor in the thigh experienced metastasis to an external iliac lymph node 7 years after marginal excision of the primary tumor, but was alive at the end of the follow-up. Table I describes the clinical outcomes reported in previous studies.

Table I. Clinical outcomes reported in previous studies of superficial CD34-positive fibroblastic tumors.

Table I.

Clinical outcomes reported in previous studies of superficial CD34-positive fibroblastic tumors.

Author, year	No.	No. with available follow-up data	Median follow-up duration (months)	No. with local recurrences and distant metastases	Outcome	(Refs.)
Carter et al, 2014	18	13	24	1 (regional lymph node metastasis)	1 ANED 12 CDF	(1)
Hendry et al, 2015	2	2	3	None	All CDF	(4)
Wada et al, 2016	1	1	3	None	CDF	(2)
Lao et al, 2017	11	11	6	None	All CDF	(3)
Li et al, 2016	1	1	24	None	CDF	(5)
Present study	1	1	5	None	CDF	–

[i] No., number of cases; ANED, alive no evidence of disease; CDF, continuous disease free.

On microscopic examination, the tumors in all patients described by Carter et al (1) were confined to the superficial fibroadipose tissues and were composed of spindle-to-epithelioid cells with an abundant granular or glassy cytoplasm arranged in fascicles and sheets. Marked pleomorphisms and a low incidence of mitotic figures were observed in all patients. On immunohistochemical examination, all tumors exhibited strong, diffuse CD34 positivity. Limited cytokeratin expression was observed in the neoplastic cells of 11 out of 16 assessed cases. Lao et al (3) suggested that it is not uncommon to misdiagnose SCPFT as a pleomorphic dermal neoplasm (particularly atypical fibroxanthoma, pleomorphic dermal sarcoma, or undifferentiated pleomorphic sarcoma/malignant fibrous histiocytoma) due to this marked pleomorphism.

The present study is a typical case of SCPFT based on the histopathological data, which are consistent with previous studies. The specific findings that CD34 was strongly positive on immunohistochemistry, and that the tumor site was superficial, assisted with the diagnosis. Although PET imaging findings for this type of tumor have not been discussed previously, the maximum standard update value on 18F-FDG PET was 2.57 in the patient of the present study; similar values are frequently observed in soft tissue tumors of intermediate malignancy (6–8). The PET findings in the current patient are considered consistent with an intermediate malignancy as described by Carter et al (1). On ultrastructural examination, the tumor cells in the present case exhibited a tendency towards fibroblast differentiation, consistent with the findings described by Hendry et al (4). It is unclear whether this feature is specific to all SCPFTs, as Hendry et al (4) were the only group aside from ours to perform ultrastructural examination. Cytogenetic studies in the present case revealed a chromosomal translocation of t(2;5)(q31;q31), according to the International System for Human Cytogenetic Nomenclature criteria (9). Juvenile-onset soft tissue sarcomas are often characterized by disease-specific fusion genes resulting from translocations, such as t(X;18) in synovial sarcomas, t(12;22) or t(2;22) in clear cell sarcomas, t(2;13) in alveolar rhabdomyosarcoma, and t(X;17) in alveolar soft part sarcomas (10–13). Additionally, Carter et al (1) suggested that SCPFT most commonly affects young to middle-aged adults. Therefore, we hypothesized that the t(2;5)(q31;q31) translocations observed in the present case suggest the existence of a chromosomal aberration specific to SCPFT. In previous studies, 3 patients with translocation-associated soft tissue tumors involving 2q31, including 2 patients with synovial sarcoma and 1 with lipoblastoma, and 1 patient with translocation-associated embryonal rhabdomyosarcoma involving 5q31, were documented (14–17).

Clinically, surgeons who are not orthopedic oncologists may perform unplanned excisions for such tumors owing to their small sizes and superficial locations; they may not accurately diagnose SCPFT owing to its rarity. As mentioned, the tumor of the present patient was initially diagnosed as an epidermoid cyst. Surgical resection was planned, and the patient almost underwent surgery at a nearby hospital 18 months prior to visiting Tottori University Hospital.

In summary, the present study described a typical case of SCPFT in the thigh of an 18-year-old man. To the best of our knowledge, this is the first study of an SCPFT in which imaging data (CT, MRI, and PET-CT) and chromosomal aberrations are described in detail for this type of tumor. It was identified that t(2;5)(q31;q31) may be a disease-specific chromosomal aberration in SCPFT. As additional characteristics of SCPFTs remain to be identified, it is important to accumulate more patients and review long-term follow-up data. This will assist in improving recognition of these tumors, and avoid misdiagnosing them as high-grade sarcomas.

Acknowledgements

The authors would like to thank Mr. T. Horie of the Technical Department, Division of Medical Science, Tottori University (Tottori, Japan), for his excellent technical assistance, and Dr S. Oda of the Department of Pathology and Experimental Medicine, Okayama University (Okayama, Japan) for performing STAT6 immunostaining.

References