1. Introduction

Skin manifestations can represent the initial clinical presentation for both T- and B-cell neoplasms. By far, primary cutaneous T-cell lymphomas are the most common hematolymphoid neoplasms of cutaneous origin, accounting for 75% of all primary cutaneous lymphoma cases [1, 2]. The remaining 25% mostly represent PCFCLs, primary cutaneous marginal zone lymphomas, and PCDLBCL-LTs. While rare, DLBCL NOS can also manifest as an isolated cutaneous disease. Identifying and diagnosing DLBCL NOS in this setting can be challenging and require clinicians to consider more common alternative diagnoses, such as PCFCL, PCDLBCL-LT, HGBCL-MYC/BLC2, B-lymphocytic leukemia/lymphoma (B-ALL), and mantle cell lymphoma (MCL) [3, 4]. As the clinical behavior and treatment of DLBCL NOS are distinct from these entities, an accurate diagnosis is critical to ensuring appropriate patient management and an optimal outcome [2].

2. Case Presentation

A 69-year-old man with a history of polymyalgia rheumatica managed with low-dose glucocorticoid therapy, chronic rhinosinusitis, and hypertensive cardiovascular disease presented to the emergency department with a subacute progressive worsening of generalized weakness. On examination, the patient had a significant truncal weakness with sitting up and rolling over in bed despite showing a full range of motion of all extremities. Palpation of the skin revealed multiple soft subcutaneous nodules on the upper extremities, abdomen, chest, and flanks. Vital signs and physical examinations were otherwise within normal limits. A complete blood count with differential was significant for macrocytic anemia with Hg of 8.7 g/dL (ref. range 13.6-17.2 g/dL) and MCV of 101 fL (ref. range 80-97 fL), thrombocytopenia with a platelet count of 91 K/μL (ref. range 160-370 K/μL), and mild leukocytosis with a WBC of 11.0 K/μL (ref. range 3.5-10.5 K/μL). Circulating absolute lymphocyte count was normal at 1,220 K/μL (ref. range 1,000-3,500 K/μL). Computed tomography including the head, neck, chest, abdomen, and pelvis revealed disseminated indeterminate subcutaneous soft tissue nodules and a low-attenuation hepatic lesion (Figure 1). Additionally, there was bilateral maxillary sinus mucosal thickening with focal bone erosion and extension into surrounding soft tissue. A subcutaneous nodule from the central abdomen was sampled by punch biopsy. The bone marrow and maxillary sinus mucosa were also biopsied.

A light microscopic examination of the subcutaneous abdominal nodule revealed mostly unremarkable epidermis, dermis, and subcutis. However, there was a focal aggregate of large atypical hematolymphoid cells within one fragment of deep adipose tissue (Figures 2(a) and 2(b)). Immunohistochemistry (IHC) performed for CD3, CD10, CD20, CD45, CD56, BCL2, CyclinD1, MUM1/IRF4, MYC, p63, PAX5, SOX10, SOX11, and TdT revealed strong and uniform staining for CD20 (Figure 2(c)), CD45, CD5 (Figure 2(d)), BCL2, BCL6 (Figure 2(e)), MUM1/IRF4 (Figure 2(f)), and PAX5. The cells were negative for all other markers (Figures 2(g) and 2(h)). Epstein-Barr virus in situ hybridization was negative. An identical population of malignant cells was found to be infiltrating separately submitted fragments of the sinus mucosa (Figure 3).

Bone marrow aspirate revealed scattered large atypical hematolymphoid cells in a background of otherwise morphologically normal trilineage hematopoiesis (Figures 4(a) and 4(b)). The bone marrow core biopsy confirmed loose aggregates of large atypical lymphoid cells with strong CD20 immunoreactivity (Figures 4(c)–4(e)). Interestingly, concurrent flow cytometry of bone marrow revealed two distinct abnormal B-cell populations: (1) a population of large lambda light chain-restricted CD5-positive B-cells, consistent with the atypical lymphoid cells noted in the aspirate (Figure 5(a)), and (2) a unique population of kappa light chain-restricted CD5-positive B-cells with a CD20-dim, light chain-dim, CD23-positive, CD200-positive immunophenotype diagnostic of chronic lymphocytic leukemia (CLL) (Figure 5(b)). The second B-cell population was most consistent with monoclonal B-cell lymphocytosis per the World Health Organization (WHO) Classification of Haematolymphoid Tumors and was favored to represent an incidental finding of unclear clinical significance.

The differential diagnoses of a primarily cutaneous high-grade B-cell neoplasm with CD5 expression included PCDLBCL-LT, HGBCL-MYC/BCL2, MCL, DLBCL NOS, and B-ALL (Table 1). To evaluate these possibilities, fluorescent in situ hybridization (FISH) for MYC gene rearrangements and the MYC/IgH fusion were performed, which was negative. This result ruled out HGBCL-MYC/BCL2. The diagnosis of PCDLBCL-LT was considered unlikely given the absence of lower extremity involvement, the male sex of the patient, the lack of a MYC translocation, and the absence of monotonous morphology. Negative IHC for TdT ruled out B-ALL, and CyclinD1 and SOX11 were both negative for IHC, which ruled out MCL. The morphologic, immunophenotypic, and clinical features of the neoplasm were all consistent with a DLBCL NOS, and cell-of-origin subtyping yielded an activated B-cell (ABC) subtype per the Hans criteria.

The diagnosis and treatment options were discussed with the patient, who opted for palliative care and died 22 days after the initial presentation.

3. Discussion

DLBCL NOS is the most common non-Hodgkin lymphoma in Western countries, accounting for 31% of adult cases [5]. Patients may present with constitutional B-symptoms (fever, night sweats, and weight loss) and/or a rapidly enlarging mass at nodal or extranodal sites [6, 7]. Disseminated disease to the bone marrow is seen in 20% of patients at diagnosis and can represent either DLBCL NOS (concordant involvement) or indolent lymphoma (discordant involvement) [8–10]. DLBCLs are phenotypically and genetically heterogeneous and are typically broadly divided into transcriptionally defined germinal center B-cell (GCB) and ABC subtypes based on cell-of-origin, with an ABC subtype conferring an adverse prognosis [11–13]. Different IHC algorithms have been developed for routine cell-of-origin subtyping. The most widely used is the Hans algorithm which scores expression of CD10, BCL6, and MUM1/IRF4 [13, 14].

Cutaneous presentations by DLBCL NOS occur in only 1.5-3.5% of cases [15, 16]. High-grade B-cell lymphoma, when encountered in the skin, raises several diagnostic considerations including PCFCL, PCDLBCL-LT, HGBCL-MYC/BCL2, and B-ALL. When positive for CD5, the differential also includes MCL (Table 1). These entities can typically be assessed via a thorough review of the clinical history and physical exam, coupled with a careful evaluation of the tissue pathology (including IHC, cytogenetics, and/or molecular testing as necessary).

PCFCL is a tumor of neoplastic follicle center B-cells that accounts for 50% of primary cutaneous B-cell lymphomas and characteristically presents as skin lesions on the head, neck, or trunk [17]. However, 15% show multifocal skin involvement. Cells appear as a mixture of centrocytes and centroblasts which may show follicular, follicular and diffuse, or diffuse architecture, usually with epidermal sparing [1]. PCFCLs are positive for the germinal center marker CD10. However, unlike nodal follicle center lymphomas, PCFCLs are negative for BCL2 [18]. When follicular architecture is not obvious, CD21 may help by highlighting associated follicular dendritic cell meshworks. When only a diffuse architecture with monotonous populations of centroblasts is present, a diagnosis of PCDLBCL-LT should be strongly considered [1]. PCFCLs have an excellent prognosis, with a 5-year survival rate greater than 95% [2]. Our patient’s lymphoma was negative for CD10, had high-grade morphology, and showed aggressive behavior with involvement of the bone marrow, which was all less consistent with PCFCL.

PCDLBCL-LT accounts for 10-20% of primary cutaneous B-cell lymphomas and is typically present on the skin of the lower extremities in elderly women (female : male ratio of 2-4 : 1) [19, 20]. Progression to disseminated disease with involvement of extracutaneous sites is common, but usually absent at diagnosis. It appears as a monotonous infiltrate in the dermis and subcutis with frequent mitotic figures and epidermal sparing [19]. The cells are positive for BCL2, MUM1/IRF4, FOXP1, MYC, and IgM, while CD10 is typically negative. The 5-year survival rate is 50%; however, recent studies incorporating rituximab have reported improved outcomes [19, 21].

HGBCL-MYC/BCL2 is a high-grade B-cell lymphoma harboring MYC and BCL2 rearrangements [4]. HGBCL-MYC/BCL2 typically presents as a disseminated disease at diagnosis in elderly individuals with a slight male predominance [22, 23]. Most HGBCL-MYC/BCL2 show morphology that is indistinguishable from DLBCL NOS and are positive for CD10, BCL2, BCL6, and MYC by IHC [13, 24]. Mandatory FISH studies confirm rearrangements involving the MYC and BCL2 genes. HGBCL-MYC/BCL2s follow an aggressive clinical course, and patients have poor outcomes with 5-survival rates of 40-50% [25].

MCL can display large cell features and should enter the diagnosis when high-grade B-cell lymphomas express CD5 [26]. They are positive for CyclinD1 by IHC, and rare CyclinD1-negative MCLs are positive for SOX11. High-grade variants of MCL have poor clinical outcomes [27]. Finally, extramedullary B-ALL should be considered in unusual presentations of apparent DLBCL NOS [28]. B-ALL expresses TdT and is usually negative for CD20 and the light chain. B-ALL is aggressive, and survival is highly age-dependent, with 20% 5-year overall survival among ages 65-74 (our patient’s age group).

In conclusion, we described a patient who presented with a nonspecific symptomatology. Multiple unexplained subcutaneous nodules seen on physical exams and imaging studies prompted the decision to biopsy. Disseminated disease with the absence of lower extremity involvement, high-grade morphology with cellular pleomorphism and diffuse architecture, negative IHC for CyclinD1, SOX11, and TdT, and absence of characteristic cytogenetic rearrangements involving MYC and BCL2, ultimately yielded a diagnosis of DLBCL NOS.

Conflicts of Interest

The authors declare no conflicts of interest.