Huge occipital spindle cell lipoma: a case report

Article information

J Korean Soc Ster Func Neurosurg. 2023;19(1):18-21
Publication date (electronic) : 2023 June 12
doi : https://doi.org/10.52662/jksfn.2023.00010
Department of Neurosurgery, Ewha Womans University Mokdong Hospital, Ewha Womans University College of Medicine, Seoul, Korea
Address for correspondence: Young Goo Kim, M.D. Department of Neurosurgery, Ewha Womans University Mokdong Hospital, Ewha Womans University College of Medicine, 1071 Anyangcheon-ro, Yangcheon-gu, Seoul 07985, Korea Tel: +82-2-2650-2645 Fax: +82-2-2650-2652 E-mail: ygkim@ewha.ac.kr
Received 2023 February 21; Revised 2023 March 17; Accepted 2023 March 17.

Abstract

Spindle cell lipoma is a subtype of lipoma first defined by Enzinger and Harvey; it accounts for <1.5% of all lipomatous tumors. We present an unusual case of a huge spindle cell lipoma. A 49-year-old man with diabetes mellitus experienced neck pain during sleep because of a huge occipital and upper posterior neck mass that had slowly grown during 4 years. We performed local excision of the tumor, and pathological findings confirmed the diagnosis of spindle cell lipoma measuring 10×9.5×5 cm. There was no recurrence 1 year after the surgery.

INTRODUCTION

Spindle cell lipoma (SCL) is an uncommon benign subcutaneous adipose tissue tumor. They most commonly appear as a slow-growing and painless mass at the shawl region (shoulder, posterior neck, and upper back) of middle-aged men (10:1 male-to-female ratio) at an average size of 4–5 cm [1,2]. Because the histological finding is similar to malignant lipomatous tumors such as liposarcoma, a precise diagnosis of SCL is essential, especially when they appear as larger masses. We present a rare case of a huge-sized occipital and upper posterior neck SCL successfully removed through local excision.

Ethical statements

This study was approved by the Institutional Review Board (IRB) of the Ewha Womans University Mokdong Hospital (IRB no: EUMC 2023-02-021). Written informed consent was obtained from the patient to publish this case report. A copy of the written consent is available for review on request.

CASE REPORT

A 49-year-old man complained of a mass in the occipital area that had slowly grown in size for 4 years (Fig. 1). He had no history of trauma or surgery in the area, and except for diabetes mellitus, he had no other medical history or allergy. On physical examination, we could check a huge palpable and movable mass that was elastic and soft. There was no tenderness, redness, or heating sensation on the mass. Computed tomography of his neck revealed a 10-×9.5-cm-sized, well-circumscribed, non-enhancing solid and fatty mass in the occipital area/posterior neck (Fig. 2).

Fig. 1.

Huge palpable mass in the occipital and posterior neck area.

Fig. 2.

(A, B) Preoperative computed tomography (CT) showing a well-circumscribed, non-enhancing, solid and fatty mass in the occipital area and upper posterior neck, measuring approximately 10×9.5×5 cm. (C, D) Postoperative CT showing total mass excision without a residual lesion.

The patient underwent surgical excision of the tumor under local anesthesia, located between the subcutaneous tissue and occipital bone/posterior neck muscles. It was well encapsulated and dissected from the adjacent tissue. There were no adhesions to adjacent tissues or vascular involvement. Until it was completely excised, including the tumor capsule, the sharp dissection was done around the lesion. The dead space was closed beneath the skin using buried, interrupted 2-0 vicryl sutures. The mass was 10×9.5×5 cm and was removed entirely without complications (Fig. 3). The patient was followed up in the outpatient department 2 weeks postoperatively with an unremarkable physical exam, with the wound completely healed without swelling or redness.

Fig. 3.

Encapsulated mass after excision, measuring approximately 10×9.5×5 cm.

On histological examination, H&E stained sections showed the lesion consists of mature adipose tissue, bland spindle cells, and ropey collagen with myxoid stroma (Fig. 4A). Immunostaining showed spindle cells for CD34-positive (Fig. 4B), S100 protein-negative, retinoblastoma 1 (Rb1) absent, and alpha-smooth muscle actin-negative. Based on these findings, a histopathological diagnosis of SCL was given. There was no recurrence 1 year after the surgery.

Fig. 4.

(A) The lesion consisted of mature adipose tissue, bland spindle cells, and ropey collagen with myxoid stroma (hematoxylin and eosin, ×200). (B) The spindle cells showed immunoreactivity for CD34 (immunohistochemistry staining, ×200).

DISCUSSION

Lipomas are slow-growing, benign adipose tumors mainly occurring in the subcutaneous tissues of the head and neck [3]. Usually, lipomas are asymptomatic, can be detected incidentally, and do not need treatment. SCL is an uncommon benign histopathological variant of lipoma that Enzinger and Harvey [1] first described in 1975 based on its characteristic histological findings characterized by collagen-rich spindle cells taking over adipocytes. SCL commonly occurs between 40 and 60 years old, are more prevalent in males [2]. Most SCL involves subcutaneous tissue of the upper back, shoulders, and posterior neck [4]. In rare cases, these tumors occur in other sites, including the face, oral cavity, and extremities [5]. In a study of 395 SCL patients, Ko et al. [2] reported that 331 (86%) occurred in men; 53 (14%) in women. SCL in women frequently occurs outside the shawl region compared with men and at a slightly younger patient age than men (median age 51 years vs. 64 years).

Grossly, SCL is a well-circumscribed, oval mass in the subcutaneous tissue and has a yellow-tan cut surface with grey-white and myxoid foci [6]. The texture is similar to typical lipomas, although it may be somewhat firmer, especially if the spindle-cell component is more dominant. Microscopically, SCL is characterized by mature adipocytes, bland spindle cells in parallel bundles, and hyalinized rope-like collagen fibers (ropy collagen) [6]. On immunohistochemistry, the spindle cells exhibit CD34, and they are negative for S100 protein. Loss of nuclear Rb1 protein expression is also a characteristic finding. On the other hand, liposarcoma, which must be differentiated from SCL, is essentially CD34-negative and S100-positive [6,7]. Both SCL and pleomorphic lipomas exhibit losses of chromosomes 13q and/or 16q-losses considered characteristic for this family of lipomas [8]. As mentioned above, most SCLs are composed of varying proportions of adipose tissue and spindle cells, which can lead to a variety of imaging findings, and it is very rare for either to be predominant. Therefore, the diagnosis of spindle-cell lipoma should be considered when one encounters a well-defined, heterogenous, fatty mass in the subcutis of a middle-aged man, especially when the mass is localized to the posterior neck [9].

Total excision, including tumor capsule, is considered as the primary treatment for SCL. In a recent study, Chen et al. [10] reported that none of the 40 patients with SCL recurred during follow-up for 2 to 105 months after surgery.

CONCLUSION

We present an unusual case of a huge-sized SCL on the occipital area and the upper posterior neck. Because of histological similarities, clinicians must confirm immunochemical findings when encountering spindle cell-associated soft tissue tumors to avoid misdiagnosis after total excision.

Notes

CONFLICTS OF INTEREST

No potential conflict of interest relevant to this article was reported.

References

1. Enzinger FM, Harvey DA. Spindle cell lipoma. Cancer 1975;36:1852–9.
2. Ko JS, Daniels B, Emanuel PO, Elson P, Khachaturov V, McKenney JK, et al. Spindle cell lipomas in women: a report of 53 cases. Am J Surg Pathol 2017;41:1267–74.
3. El-Monem MH, Gaafar AH, Magdy EA. Lipomas of the head and neck: presentation variability and diagnostic work-up. J Laryngol Otol 2006;120:47–55.
4. Piattelli A, Perrotti V, Fioroni M, Rubini C. Spindle cell lipoma of the floor of the mouth: report of a case. Auris Nasus Larynx 2005;32:205–7.
5. Fletcher CD, Martin-Bates E. Spindle cell lipoma: a clinicopathological study with some original observations. Histopathology 1987;11:803–17.
6. Van Treeck BJ, Fritchie KJ. Updates in spindle cell/pleomorphic lipomas. Semin Diagn Pathol 2019;36:105–11.
7. Biagiotti J, Khan K, Ayrapetyan M, Wood J, Bhatt N. Fat-free spindle cell lipoma of the scalp: lipoma without a lipogenic component. J Craniofac Surg 2022;33:e429–31.
8. Thompson LD. Spindle-cell lipoma. Ear Nose Throat J 2009;88:992–3.
9. Bancroft LW, Kransdorf MJ, Peterson JJ, O’Connor MI. Benign fatty tumors: classification, clinical course, imaging appearance, and treatment. Skeletal Radiol 2006;35:719–33.
10. Chen S, Huang H, He S, Wang W, Zhao R, Li L, et al. Spindle cell lipoma: clinicopathologic characterization of 40 cases. Int J Clin Exp Pathol 2019;12:2613–21.

Article information Continued

Fig. 1.

Huge palpable mass in the occipital and posterior neck area.

Fig. 2.

(A, B) Preoperative computed tomography (CT) showing a well-circumscribed, non-enhancing, solid and fatty mass in the occipital area and upper posterior neck, measuring approximately 10×9.5×5 cm. (C, D) Postoperative CT showing total mass excision without a residual lesion.

Fig. 3.

Encapsulated mass after excision, measuring approximately 10×9.5×5 cm.

Fig. 4.

(A) The lesion consisted of mature adipose tissue, bland spindle cells, and ropey collagen with myxoid stroma (hematoxylin and eosin, ×200). (B) The spindle cells showed immunoreactivity for CD34 (immunohistochemistry staining, ×200).