Intra-abdominal inflammatory pseudotumor-like follicular dendritic cell sarcoma associated with paraneoplastic pemphigus: A case report and review of the literature

Abstract

BACKGROUD

Follicular dendritic cell (FDC) sarcomas are rare neoplasms that occur predominantly in the lymph nodes. They can also occur extranodally. Extranodal FDC sarcomas most commonly present as solitary masses. Inflammatory pseudotumor (IPT)-like FDC sarcomas, a subcategory of FDC sarcomas, are rarer than other sarcoma subtypes. They are composed of spindle or ovoid neoplastic cells and exhibit an admixture of plasma cells and prominent lymphoplasmacytic infiltration. Paraneoplastic pemphigus (PNP), also known as paraneoplastic autoimmune multiorgan syndrome, is a rare autoimmune bullous disease that is associated with underlying neoplasms. PNP has a high mortality, and its early diagnosis is usually difficult.

CASE SUMMARY

We describe a 27-year-old woman who presented with stomatitis, conjunctivitis, and skin blisters and erosions as her first symptoms of PNP with an intra-abdominal IPT-like FDC sarcoma. The patient underwent surgical tumor resection and received tapering oral corticosteroid treatment. She showed no recurrence at the 1-year follow-up.

CONCLUSION

IPT-like FDC sarcomas are rare underlying neoplasms that have an uncommon association with PNP. PNP-associated FDC sarcomas predominantly occur in intra-abdominal sites and suggest a poor prognosis. Surgical resection is an essential and effective treatment for PNP and primary and recurrent FDC sarcomas.

Key Words: Inflammatory pseudotumor-like follicular dendritic cell sarcoma, Paraneoplastic pemphigus, Follicular dendritic cell sarcoma, Resection, Case report

Core tip: To date, 32 cases of paraneoplastic pemphigus (PNP)-associated follicular dendritic cell (FDC) sarcomas have been reported in the English literature. Inflammatory pseudotumor-like FDC sarcoma was described as an underlying neoplasm of PNP in only two cases. Here, we report a case that PNP was the patient’s first symptom of an intra-abdominal inflammatory pseudotumor-like FDC sarcoma, and review the related literature.

INTRODUCTION

Follicular dendritic cell (FDC) sarcoma was first described in 1986 by Monda et al[1] as a nonlymphomatous lymph node malignancy with features suggesting a FDC origin. It is classified into two types: (1) Conventional FDC sarcomas that are histologically characterized by spindle cell proliferation with fascicles, trabecular, or diffuse sheets; and (2) Inflammatory pseudotumor (IPT)-like FDC sarcomas, an entity proposed by Cheuk et al[2] in 2001, which are characterized by dispersed spindle or ovoid tumor cells against a background of abundant lymphocytes and plasma cells. However, in contrast to conventional FDC sarcomas, IPT-like FDC sarcomas predominantly arise in intra-abdominal sites, especially the liver and spleen. Paraneoplastic pemphigus (PNP), which was first described in 1990, is a rare and life-threatening mucocutaneous autoimmune disease that is associated with underlying neoplasms, especially lymphoproliferative disorders[3]. A total of 32 cases of FDC sarcomas associated with the occurrence of PNP have been previously reported (Table 1)[4-30]. Only two case wherein an IPT-like FDC sarcoma is an underlying neoplasm of PNP have been described[20,31]. Here, we report a 27-year-old woman who presented stomatitis, conjunctivitis, and polymorphic cutaneous lesions, which are consistent with the features of PNP, as her first symptoms of intra-abdominal IPT-like FDC sarcoma, and review the related literature. This work intends to serve as a reference for the correct identification of this disease by clinicians. It also aims to broaden clinicians’ understanding of this kind of tumor, PNP, and their rare relationship.

Table 1 Summary of 32 cases of paraneoplastic pemphigus-associated follicular dendritic cell sarcoma.

Ref.	Sex/age	Tumor pathology	Location	Maximum diameter (cm)	Clinical manifestations	Treatments	Follow-up
Walters et al[4]	M/48	FDCS	Anterior mediastinum	NA	Lichenoid skin lesions, BO, MG	Tumor resection, multiple immunosuppressive therapies	Progressive respiratory disease
	M/88	FDCS	Retropharynx	8	Mucosal lichenoid erosions	Tumor resection	DOD within 1 yr, status unknown
	F/59	FDCS	Axillary lymph node	NA	Lichenoid skin lesions, mucocutaneous blisters, BO	Tumor resection	DOD within 6 mo
	M/23	FDCS associated with CD	Cervical lymph node	NA	Mucosal lichenoid erosions, BO	Partial tumor resection and residual mass was radiated	Tumor recurrence and DOD within 2 yr
Lu et al[5]	F/49	FDCS	Pancreatic tail	6	Stomatitis, MG, pulmonary infection	Tumor resection, antifungal and anti-infection therapies	DOD 12 d after surgery
Jonkman et al[6]	F/35	FDCS	Intra-abdomen	NA	Stomatitis, punctate keratoses with central ulceration on the palms and soles.	Tumor resection and intensive immunosuppression	DOD with respiratory failure
Akel et al[7]	M/39	FDCS	Intra-abdomen	18	Lichenoid skin lesions, mucocutaneous blisters, febrile neutropenia	Tumor resection and high-dose steroids	DOD with severe pneumonia and acidosis
Wang et al[8]	F/56	FDCS associated with CD	Retroperitoneum	10	Stomatitis, polymorphous skin lesions, BO	Tumor resection, IVIg and steroid therapies	Alive at 4 yr follow-up
Wang et al[9]	F/27	FDCS	Retroperitoneum	8	Stomatitis, conjunctivitis, lichenoid skin lesions	Tumor resection	Tumor recurrence 5 yr after surgery
Su et al[10]	M/43	FDCS	Retroperitoneum	5	Stomatitis, lichenoid skin lesions	Tumor resection and lymphadenectomy, IVIg and steroid therapies	DOD with multiple organ failure
Chow et al[11]	M/62	FDCS	Anterior mediastinum	7.5	Stomatitis, conjunctivitis, mucocutaneous blisters	Right thoracotomy and tumor resection, adjuvant radiotherapy	DOD with respiratory failure
Garza-Chapa et al[12]	M/20	FDCS	Right-side mediastinum	7	Stomatitis, conjunctivitis, lichenoid skin lesions	Right thoracotomy and tumor resection, chemotherapy with R-CVP (rituximab, cyclophosphamide, vincristine, prednisone)	Resolution of skin lesions and no evidence of tumor recurrence at 1-yr follow-up
Streifel et al[13]	M/72	FDCS	Right-side mediastinum	NA	Stomatitis, conjunctivitis, and glans penis involvement, lichenoid skin lesions, MG	Thymectomy and partial pericardiectomy, rituximab, IVIg, steroids and mycophenolate mofetil	Improvement at 9-mo follow-up
Kim et al[14]	M/68	FDCS	Small bowel mesentery	9	Abdominal palpable mass, stomatitis, conjunctivitis, MG	Tumor resection	Metastatic tumors found in the liver 1 yr after surgery; DOD within 2 yr
Seishima et al[15]	F/64	FDCS	Retroperitoneum and small intestine	15	Stomatitis, conjunctivitis, severe skin erosions	Tumor resection and steroid therapy	Tumor recurrence; DOD with fungal infective embolisms in the lungs
Liu et al[16]	F/54	FDCS	Retroperitoneum	10.8	Stomatitis, Lichenoid skin lesions	Tumor resection, systemic corticosteroid, and cyclosporine therapies	DOD with respiratory failure
Baghmar et al[17]	M/20	FDCS	Right hemipelvis	6	Stomatitis, conjunctivitis, lichenoid skin lesions	Unresectable, chemotherapy with rituximab, cyclophosphamide, adriamycin, vincristine, and prednisolone	DOD with respiratory pseudomonas infections
Hwang et al[18]	F/46	FDCS	Liver	16	Abdominal pain, Stomatitis, lichenoid skin lesions	Tumor resection, rituximab and ciclosporin therapies	Tumor recurrence 1 yr after surgery; DOD with pneumonia
Lee et al[19]	M/67	FDCS associated with CD	Small bowel mesentery	NA	Stomatitis, conjunctivitis, MG	Tumor resection, IVIg, prednisolone, and cyclosporine therapies	Metastatic tumors found in the liver 1 yr after surgery
Zhao et al[20]	F/28	IPT-like FDCS	Intra-abdomen	9	Stomatitis, blisters and erosions of the underarm, groin and perineum, and labia majora, BO	Tumor resection	Improvement after surgery
Sugiura et al[21]	M/28	FDCS associated with CD	Left retroperitoneum	7.7	Stomatitis, polymorphic cutaneous lesions, papillomatous hyperplasia on the tongue	Tumor resection, chemotherapy of COP (cyclophosphamide, vincristine, and prednisolone)	Skin lesions healed completely except for the papillomatous hyperplasia on the tongue, and follow-up is not clear
Marzano et al[22]	F/53	FDCS	Right retroperitoneum	9	Stomatitis, conjunctivitis, lichenoid skin lesions, dyspnea	Tumor resection, systemic corticosteroid and IVIg therapies	DOD with respiratory failure within 2 yr
Meijs et al[23]	M/60	FDCS	Mediastinum	6	Stomatitis, conjunctivitis, mucocutaneous blisters and erosions, BO	Tumor resection, chemotherapy with rituximab, IVIg, plasmapheresis, corticosteroid, azathioprine and cyclophosphamide	DOD with respiratory failure
Lee et al[24]	M/66	FDCS associated with CD	Right retroperitoneum	12	Stomatitis, conjunctivitis, mucocutaneous blisters and erosions, lichenoid skin lesions	Tumor resection and antibiotics therapy	DOD with sepsis 8 d after surgery
Choi et al[25]	F/39	FDCS	NA	NA	Stomatitis, mucocutaneous blisters and erosions	Tumor resection	Alive for 5 yr, and skin lesions healed except for oral persistent mucositis
Zhang et al[26]	M/20	FDCS associated with CD	NA	NA	Stomatitis, conjunctivitis and genital involvement, skin blisters	Tumor resection	Alive for 3 yr without recurrence
	M/16	FDCS associated with CD	NA	NA	Stomatitis, conjunctivitis and genital involvement, skin blisters	Tumor resection	DOD with severe infections 2 wk after surgery
Yamada et al[27]	M/68	FDCS	Retroperitoneum	NA	Stomatitis, conjunctivitis and genital involvement, polymorphic cutaneous lesions	Tumor resection, plasmapheresis, and steroid pulse therapies	DOD with septicemia 2 mo after surgery
Ogawa et al[28]	M/28	FDCS	Retroperitoneum	NA	Stomatitis, skin blisters and erosions	Partial resection, IVIg, chemotherapy with cyclophosphamide, vincristine, and prednisolone therapies	Alive for 3 yr, and skin lesions healed except for oral persistent mucositis
Raco et al[29]	F/61	FDCS associated with CD	Intra-abdomen	10	Stomatitis, lichenoid skin lesions, dyspnea	Previous: splenectomy and chemotherapy 3 yr agoRecent: IVIg, rituximab, steroid and antibiotic therapies	Tumor metastasis or recurrence; DOD with respiratory failure
Rice et al[30]	F/41	FDCS	Retroperitoneum	8	Stomatitis, conjunctivitis, lichenoid skin lesions dyspnea,	Tumor resection, IVIg, systemic corticosteroid, rituximab, and daclizumab therapies	Progressive respiratory failure
Wang et al[31]	F/60	IPT-like FDCS	Left axillary and cervical lymph nodes	6.4	Stomatitis, polymorphic cutaneous lesions, MG, dyspnea	Tumor resection, IVIg, steroid, and rituximab therapies	DOD with multiple organ failure
Present case	F/27	IPT-like FDCS	Intra-abdomen	9	Stomatitis, conjunctivitis, skin blisters and erosions, mild dyspnea	Tumor resection, tapering corticosteroid	No evidence of tumor recurrence at 1-yr follow-up

M: Male; F: Female; DOD: Dead of disease; NA: Not available; FDCS: Follicular dendritic cell sarcoma; CD: Castleman disease; BO: Bronchiolitis obliterans; MG: Myasthenia gravis; IVIg: Intravenous immunoglobulin.

CASE PRESENTATION

Chief complaints

A 27-year-old Chinese woman presented with complaints of painful desquamative stomatitis, conjunctivitis for 2 mo (Figure 1A), and polymorphic skin lesions on the trunk (Figure 1B) for half a month.

Figure 1 Diffuse lips and mucosal erythema and erosions (A), erythema and loose blisters on the trunk (B), intraepidermal acantholysis and blisters (orange arrow; HE × 40) (C), and linear deposition of C3 in the basal stratum of skin (orange arrow; × 100) (D).

History of present illness

Oral blisters and erosions occurred first, and skin lesions, including erythema, vesicles, and erosions, developed on the trunk subsequently. The patient had no abdominal discomfort or other gastrointestinal symptoms.

Physical examination upon admission

Oral blisters and erosions involved mucus membranes, the tongue, and lips. The vesicles on the trunk were loose and positive for the Nikolsky sign (a dermatological examination method of acanthocyte loosening that is performed to check whether blisters and bullae are located inside or under the epidermis).

Laboratory examinations

Enzyme-linked immunosorbent assay revealed increased concentrations of circulating serum autoantibodies against desmoglein-1 and desmoglein-3 (two kinds of pemphigus antibodies).

Imaging examinations

For the patient complained of mild dyspnea, a chest computed tomography (CT) scan was performed, which revealed mild bronchiolitis obliterans on the patient’s lungs. Besides, it happened to scan an iso-dense, well-circumscribed mass in the upper abdominal area (Figure 2A and B).

Figure 2 Computed tomography scan showed that there was an iso-dense, well-circumscribed mass (orange arrow) in the upper abdominal area. A: Axial section; B: Coronal section.

Histological examinations

Skin lesion biopsy showed intraepidermal acantholysis and blisters (Figure 1C). Moreover, C3 was detected in the basal stratum through direct immunofluorescence (Figure 1D). The postoperative pathology of the tumor showed that spindle vacuolar tumor cells with mild cellular atypia were distributed against a background of abundant small lymphocytes, especially in pseudofollicles (Figure 3A). Some abnormal nuclear fissions were observed (Figure 3B), and cells resembling Reed–Sternberg cells were captured at times. Immunohistochemical studies revealed that the tumor cells were positive for CD21 (Figure 3C), CD68, and Ki-67 (maximally 20% to 30%) and negative for CK, CD3, HMB-45, CD20, CD30, CD34, CD117 (Figure 3D), and anaplastic lymphoma kinase.

Figure 3 The tumor tissue had a clear boundary (HE × 20) (A), spindle tumour cells were distributed in the background of abundant small lymphocytes (HE × 100) (B), the neoplastic cells were strong positive for CD21 (× 200) (C), and the neoplastic cells were negative for CD117 (× 100) (D).

FINAL DIAGNOSIS

PNP associated with IPT-like FDC sarcoma.

TREATMENT

Before the diagnosis of IPT-like FDC sarcoma, the patient received treatments of methylprednisolone combined with cyclophosphamide and showed improvement but shortly relapsed. After the diagnosis of IPT-like FDC sarcoma, the patient underwent surgical resection of the sarcoma. The resected tumor, which had dimensions of 9 cm × 6 cm × 6 cm, was solid and circumscribed. Gradually tapering methylprednisolone treatment was continued as a conservative adjuvant therapy to ensure that the patient’s PNP was controlled.

OUTCOME AND FOLLOW-UP

When the patient previously received drug treatments for pemphigus, she improved but her symptoms relapsed shortly. By contrast, after the surgical resection of her sarcoma, the patient was free from pemphigus symptoms. PNP and IPT-like FDC sarcoma showed no recurrence at the 1-year follow-up (Figure 4A and B).

Figure 4 Mucosal and skin lesions had disappeared, leaving lichenoid hyperpigmentation behind (A and B).

DISCUSSION

In the case that we described, the existence and disappearance of PNP had a direct relationship with IPT-like FDC sarcoma. This relationship adequately illustrated an extremely unusual association of IPT-like FDC sarcoma with PNP. Sarcoma is an underlying malignancy in approximately 6% of PNP cases; it is involved in leiomyosarcomas, liposarcomas, malignant nerve sheath tumors, poorly differentiated sarcomas, reticulum cell sarcomas, dendritic cell sarcomas, and inflammatory myofibroblastic tumors[32]. The occurrence of PNP with IPT-like FDC sarcoma is rare. To date, 32 cases of PNP-associated FDC sarcomas have been reported in the English literature (Table 1). Given that IPT-like FDC sarcoma was described as an underlying neoplasm of PNP in only two cases[20,31], our presentation is extremely rare. PNP-associated FDC sarcomas tend to show an Asian preference (21/32), especially among Eastern Asians. Previously reported cases involved 18 males and 14 females (male/female ratio of 1.3: 1) with a mean age of 47 years (range, 16-88 years). The locations of FDC sarcomas were the mediastinum (5/29), cervix (3/29), axillary lymph nodes (2/29), and intra-abdominal sites (20/29). Locations were not mentioned in three cases. Nearly 70% cases of PNP-associated FDC sarcomas occurred in intra-abdominal sites, even though FDC sarcomas themselves predominantly occur in the cervical and axillary lymph nodes. This characteristic suggests that intra-abdominal FDC sarcomas may indicate a poor prognosis. Furthermore, in six cases, FDC sarcomas caused PNP were coexisting with myasthenia gravis (MG)[4,5,13,14,19,21]. Paraneoplastic neurologic syndromes are even rarer than other syndromes, occurring in approximately 0.01% of patients with cancer[33]. PNP was the first autoimmune disease that was demonstrated to be associated with FDC sarcoma[24]. Subsequently, Hartert et al[34] first reported in 2010 that FDC sarcoma is associated with MG without PNP. What’s more, Sandri et al[35] once reported that paraneoplastic arthritis is the first symptom of IPT-like FDC sarcoma. FDC sarcoma is one of the underlying risk factors for developing paraneoplastic autoimmune diseases, which show a high mortality rate. Its early and correct identification by clinicians is crucial.

Previous reports have revealed that diseases associated with PNP predominantly underlie B-cell lymphoproliferative diseases, for example, non-Hodgkin lymphomas, chronic lymphocytic leukemia, and Castleman disease, such that 84% of neoplasms are associated with PNP[31]. Interestingly, we found that Castleman disease was involved in eight cases of PNP-associated FDC sarcoma (Table 1)[4,8,19,21,24,26,29]. In China, PNP is frequently found in association with Castleman’s tumors[36]. Some researchers assumed that FDC sarcoma arose from hyaline vascular Castleman disease, possibly through a mechanism involving epidermal growth factor receptors[37]. A recent genetic study has suggested that FDC sarcomas associated with unicentric hyaline-vascular Castleman disease show mutations and copy number changes in known oncogenes, tumor suppressors, and chromatin remodeling genes[38]. In addition, histologically, indolent T-lymphoblastic proliferation is frequently found in FDC sarcomas and shows an association with paraneoplastic autoimmune multiorgan syndrome; this association suggests that neoplastic follicular dendritic cells can recruit or foster the proliferation of immature T cells, which may lead to the occurrence of PNP[4,22]. In the present study, we failed to detect the immunohistochemistry of TdT, which is a necessary index for later studies. However, the patient’s manifestations improved and her serum autoantibody titers gradually decreased after tumor resection. We thus hypothesized that B lymphocytes also have a notable role in this associated tumor. Zhu’s research team used a specific peptide to probe the specific immunoglobulin receptors on tumor B lymphocytes from patients with PNP and confirmed that associated tumors can produce autoantibodies against antigens in the epidermis[39]. The relationships among immature T cells–B cells–PNP in FDC sarcomas and other trigger tumors require further studies.

FDC sarcomas are low-grade tumors. Further studies with long follow-up periods have recently indicated that FDC sarcomas are at least intermediate-grade tumors given their local recurrence and occasional distant metastases[40]. PNP-associated FDC sarcomas suggest a poor prognosis and high mortality rate. The risk factors related to mortality are severe infections, such as sepsis and infectious pneumonia; lung bronchiolitis obliterans; multiple organ dysfunction; and tumor recurrences or metastases (Table 1). The stabilization of vital parameters, the evaluation of any underlying malignancy, the accurate diagnosis of PNP, the removal and medical therapy of the trigger tumor, and the treatment of PNP are six indispensable steps to improve the management of patients with PNP[41]. We reckoned that the early treatment and management of PNP helped prevent serious infection and degeneration in the present case. However, PNP, especially stubborn oral mucosa lesions that are observed in most cases, is considered refractory to conventional medical treatments compared with other types of pemphigus. Unified criteria for the therapy and evidence-based treatment of PNP remain lacking. The early detection and resection of trigger tumors are essential for the treatment of PNP since they may produce autoantibodies to impair the epidermis[39]. The 31 patients that we reviewed above underwent complete (29/31) or partial (2/31) surgical resection. Only one case had a tumor that was found to be unresectable during exploratory laparotomy[17]. Surgical resection seems to be the first choice for the treatment of primary and recurrent FDC sarcomas, whereas the role of adjuvant radiotherapy or chemotherapy has not been well defined[42]. A recent study revealed that the local recurrence and distant metastasis rate of IPT-like FDC sarcomas is approximately 17%[43], whereas that of conventional FDC sarcomas is 40%–50%, suggesting that IPT-like FDC sarcomas are a more indolent variant of FDC sarcomas. Our patient showed no recurrence or metastasis of the sarcoma at the 1-year follow-up. Continued long-term follow is required to obtain improved insight into these two diseases.

CONCLUSION

IPT-like FDC sarcomas are rare underlying neoplasms that have an uncommon association with PNP. To date, only 32 cases of PNP-associated FDC sarcomas have been reported in the English literature. Intra-abdominal FDC sarcomas may suggest a poor prognosis. The immature T cells and B cells of FCD sarcomas might play roles in PNP development, and the mechanisms of these roles require further studies. Surgical resection is an essential and effective treatment for PNP and primary and recurrent FDC sarcomas. IPT-like FDC sarcomas seem to be more indolent than conventional FDC sarcomas, and long-term follow-up is required.

ACKNOWLEDGEMENTS

The authors would like to thank the Pathology Department of Dermatology Hospital, Southern Medical University for their contributions to the acquisition of histopathology images.