Oral manifestations of HIV disease are common and include oral lesions and novel presentations of previously known opportunistic diseases.(1,2) Careful history taking and detailed examination of the patient's oral cavity are important parts of the physical examination,(3,4) and diagnosis requires appropriate investigative techniques. Early recognition, diagnosis, and treatment of HIV-associated oral lesions may reduce morbidity.
This chapter is an overview of oral lesions most frequently associated with HIV disease (Table
1).(5,6) The presence of these lesions may be an early diagnostic indicator of immunodeficiency and HIV infection, may change the classification of the stage of HIV infection, and is a predictor of the progression of HIV disease.(7-9)
| FUNGAL LESIONS|
Oral candidiasis is most commonly associated with Candida albicans, although other species, such as C. glabrata and C. tropicalis, are frequently part of the normal oral flora. A number of factors predispose patients to develop candidiasis: infancy, old age, antibiotic therapy, steroid and other immunosuppressive drugs, xerostomia, anemia, endocrine disorders, and primary and acquired immunodeficiency. Candidiasis is a common finding in people with HIV infection. Reports describe oral candidiasis during the acute stage of HIV infection,(10) but it occurs most commonly with falling CD4+ T-cell count in middle and late stages of HIV disease. Several reports indicate that most persons with HIV infection carry a single strain of Candida during clinically apparent candidiasis and when candidiasis is quiescent.(11)
| Clinical Features|
The clinical appearances of oral candidiasis vary. The most common presentations include pseudomembranous and erythematous candidiasis, which are equally predictive of the development of AIDS,(12) and angular cheilitis. These lesions may be associated with a variety of symptoms, including a burning mouth, problems eating spicy food, and changes in taste (Figure
2). All three of these common forms may appear in one individual.
| Pseudomembranous Candidiasis (Thrush)|
Characteristic creamy white, removable plaques on the oral mucosa are caused by overgrowth of fungal hyphae mixed with desquamated epithelium and inflammatory cells. The mucosa may appear red when the plaque is removed. This type of candidiasis may involve any part of the mouth or pharynx.
| Erythematous Candidiasis|
Erythematous candidiasis appears as flat, red patches of varying size. It commonly occurs on the palate and the dorsal surface of the tongue. Erythematous candidiasis is frequently subtle in appearance and clinicians may easily overlook lesions, which may persist for several weeks if untreated.
| Angular Cheilitis|
Angular cheilitis appears clinically as redness, ulceration, and fissuring, either unilaterally or bilaterally at the corners of the mouth. It can appear alone or in conjunction with another form of candidiasis.
| Hyperplastic Candidiasis|
This type of candidiasis is unusual in persons with HIV infection. The lesions appear white and hyperplastic. The white areas are due to hyperkeratosis and, unlike the plaques of pseudomembranous candidiasis, cannot be removed by scraping. These lesions may be confused with hairy leukoplakia. Diagnosis of hyperplastic candidiasis is made from the histologic appearance of hyperkeratosis and the presence of hyphae. Periodic acid-Schiff (PAS) stain is often used to demonstrate hyphae.
| Differential Diagnosis|
Erythematous candidiasis should be differentiated from other red lesions, such as Kaposi's sarcoma or erythroplakia. Histologically, oral candidiasis contains Candida hyphae in the superficial epithelium when viewed under a PAS stain. The inflammatory responses often associated with Candida infection may be absent in immunocompromised patients. The creamy white plaques of pseudomembranous candidiasis are removable; the white lesions of hairy leukoplakia are nonremovable.
Candida is a commensal organism in the oral cavity. Candidiasis is diagnosed by its clinical appearance and by detection of organisms on smears. Smears taken from clinical lesions are examined using potassium hydroxide (KOH), PAS, or Gram's stain. Smears are taken by gently drawing a wooden tongue depressor across the lesion. The specimen is then transferred into a drop of KOH on a glass slide and protected by a cover slip. The smear is examined under the microscope and Candida is detected by finding hyphae and blastospores. Hyphae and spores are only seen in smears from lesions and are rarely seen in the healthy individual in the carrier state. Cultures are grown on specific media, such as Sabouraud's agar; they may be positive and yet reveal very low colony counts. This probably represents a carrier state rather than active infection.(13) Culture is useful for establishing the Candida species but may not be useful for diagnosis.
Oral candidiasis may be treated either topically or systemically.(14) Treatment should be maintained for 7 days. Response to treatment is often good; oral lesions and symptoms may disappear in a fairly short period (ranging from 2 to 5 days), but relapses are common because of the underlying immunodeficiency. As with other causes of oral candidiasis, recurrences are common if the underlying problem persists.
| Topical Treatment|
Topical treatments are preferred because they limit systemic absorption, but the effectiveness depends entirely on patient compliance. Topical medications require that the patient hold medications in the mouth for 20 to 30 minutes. If the patient uses formulations containing sweetening agents for long periods, consider as concurrent treatment daily fluoride rinses (e.g., ACT or Fluorigard, available as over-the-counter preparations) for 1 minute once a day and then expectorated.
Clotrimazole is an effective topical treatment (one oral troche [10-mg tablet]) when dissolved in the mouth five times daily. Used less frequently, one vaginal troche can be dissolved in the mouth daily. Nystatin preparations include a suspension, a vaginal tablet, and an oral pastille. Regimens are nystatin vaginal tablets (one tablet, 100,000 units, dissolved in the mouth three times a day), or nystatin oral pastille (available as a 200,000-unit oral pastille, one or two pastilles dissolved slowly in the mouth five times a day). Nystatin suspension has a high sugar content and cannot be held in the mouth long enough to be effective. Topical creams and ointments containing nystatin, ketoconazole, or clotrimazole may be useful in treating angular cheilitis. Another therapeutic choice is amphotericin B (0.1 mg/ml). Five to 10 ml of oral solution is used as a rinse and then expectorated three to four times daily.
| Systemic Treatment|
Several agents are effective for systemic treatment. Ketoconazole (Nizoral) is a 200-mg tablet taken with food once daily. Patient compliance is usually good. Careful monitoring of liver function is necessary for long-term use because of reported side effects, including hepatotoxicity. Lack of efficacy of ketoconazole may occur because of poor absorption in those with an abnormally high gastric pH.
Fluconazole (Diflucan) is a triazole antifungal agent effective in treating candidiasis (100-mg tablet taken once daily for 2 weeks).(15) Several studies(15) suggest fluconazole is effective as a prophylactic agent, although the most effective prophylaxis dosing regimen is still unclear. Numerous reports,(16) however, describe oral and esophageal candidiasis failing to respond to treatment with fluconazole, and in some of these cases investigators isolated resistant strains.(16,17) Itraconazole (100-mg capsules) may be used for the treatment of oral candidiasis (200 mg daily orally for 14 days).(18) Itraconazole oral suspension is now available (200 mg daily for 2 weeks. Salivary levels of itraconazole are maintained for several hours after administration.
Ketoconazole, fluconazole, and itraconazole may interact with other medications including rifampicin, phenytoin, cyclosporin A, terfenadine, digoxin, coumarin-like medications, and oral hypoglycemic medications.
| Prognostic Significance|
Both erythematous and pseudomembranous oral candidiasis are associated with increased risk for the subsequent development of opportunistic infections classifying the patient as having AIDS as defined by the Centers for Disease Control (CDC).(19)Several studies have shown a statistical correlation between frequency of oral candidiasis in HIV infection and falling CD4+ T-cell counts.(20)
Histoplasmosis may initially present in the oral cavity. These lesions appear as ulcerations that can affect any mucosal surface. Diagnosis requires biopsy.(21) Histoplasmosis is discussed extensively in Chapter 6.9.
| Cryptococcus Neoformans|
A report described Cryptococcus neoformans causing an ulcerated mass in the hard palate of a patient with a previous history of Pneumocystis carinii pneumonia. A biopsy of the palatal ulcer made the diagnosis.(22)
| VIRAL LESIONS|
| Herpes Simplex|
Herpes simplex causes both primary and secondary or recurrent disease in the oral cavity. Primary herpetic gingivostomatitis commonly occurs in children and young adults and may be followed by frequent recurrences. Following the primary episode, the virus becomes latent in the trigeminal ganglion. Recurrent oral herpes occurs at any age extraorally or intraorally.
| Clinical Features|
Recurrent herpes labialis occurs on the vermilion border of the lips. The patient may report a history of itching or pain, followed by the appearance of small vesicles. These rupture and form crusts. Recurrent intraoral herpes appears as clusters of painful small vesicles that rupture and ulcerate and usually heal within 1 week to 10 days. The lesions usually occur on the keratinized mucosa, such as the hard palate and gingiva, although lesions may arise on the dorsal surface of the tongue.
| Differential Diagnosis|
Rising antibody titers from initial and convalescent sera confirm primary herpetic gingivostomatitis. Examining smears of lesions (treated with Papanicolaou stain) for multinucleated giant cells confirms recurrent herpes. It is possible to demonstrate herpes simplex type 1 or type 2 by applying monoclonal antibodies to smears from the lesions (the Syva Kit, Syva Corporation, Palo Alto, CA).(23) Swabs taken from fluid-filled vesicles may grow herpes simplex in culture if vesicles are a few days or less old. Clinicians can distinguish between recurrent intraoral herpes simplex lesions, which always occur on keratinized mucosa (such as the hard palate and gingiva), and recurrent aphthous ulcers, which always appear on nonkeratinized mucosa. Recurrent intraoral herpes may appear more frequently in HIV-infected patients. The lesions may be painful and slow to heal.
No treatment will permanently eradicate oral herpes simplex infections, but acyclovir may shorten the healing time for individual episodes. The optimum oral dosage of acyclovir is 1,000 to 1600 mg daily for 7 to 10 days. Topical acyclovir is not useful for treating intraoral lesions and may not be effective for lesions on the lips. Recurrent outbreaks of acyclovir-resistant herpes have been reported, including a case involving the facial skin, lips, nose, and mouth. In this case, the lesions resolved after treatment with foscarnet.(24) Phosphonoformate may also prove effective.
| Prognostic Significance|
There is no known association between recurrent intraoral herpes and more rapid progression of HIV disease. However, there is a clinical impression that recurrent herpes simplex infections may be more common in patients with symptomatic HIV disease.(25)
| Human Papillomavirus Lesions|
Oral warts, papillomas, skin warts, and genital warts are associated with the human papillomavirus (HPV).(1) Lesions caused by HPV are common on the skin and mucous membranes of persons with HIV disease. Anal warts have frequently been reported among homosexual men. Because the HPV types found in oral lesions in HIV-infected persons are different from the HPV types associated with anogenital warts, clinicians should probably not use the term condyloma acuminata to describe oral HPV lesions.
| Clinical Features|
HPV lesions in the oral cavity may appear as solitary or multiple nodules. They may be sessile or pedunculated and appear as multiple, smooth-surfaced raised masses resembling focal epithelial hyperplasia or as multiple, small papilliferous or cauliflower-like projections (Figure
3). I have identified HPV types 7, 13, and 32 in some of these oral warts.(26) Malignant transformation of HPV oral lesions has not been reported, but the identification of four new HPV types in these lesions warrants further study.
| Differential Diagnosis|
A biopsy is necessary for histologic diagnosis.
There is no known association between oral HPV lesions and more rapid progression of HIV disease, but oral warts are seen more commonly in HIV-infected persons than in the general population.
Oral HPV lesions can be removed surgically using local anesthetic. Carbon dioxide laser surgery can remove multiple flat warts, but relapses occur and several repeat procedures may be necessary.
Oral ulcers caused by cytomegalovirus (CMV) have been reported.(27) These ulcers can appear on any mucosal surface and may be confused with aphthous ulcers,(28) necrotizing ulcerative periodontitis (NUP),(29) and lymphoma. Unlike aphthous ulcers, however, which usually have an erythematous margin, CMV ulcers appear necrotic with a white halo.(30) Diagnosis of CMV ulcers is made from a biopsy. Immunohistochemistry may be helpful.
CMV ulcers in the oral cavity usually occur in individuals with disseminated CMV disease. Therefore, diagnosis of CMV-infected oral ulcers should be followed by examination for the systemic disease. CMV ulcers resolve when ganciclovir is used to treat CMV disease.
| Hairy Leukoplakia and Epstein-Barr Virus|
Oral hairy leukoplakia (HL), which presents as a nonmovable, corrugated or "hairy" white lesion on the lateral margins of the tongue, occurs in all risk groups for HIV infections, although less commonly in children than in adults.(31-33) HL occurs in about 20% of persons with asymptomatic HIV infection and becomes more common as the CD4+ T-cell count falls.(34) HL is in group 4, category C2 of the original Centers for Disease Control (CDC) definition of AIDS and in B3 of the 1993 criteria.(35,36) No report describes HL in mucosal sites other than the mouth.(37) HL has occurred in non-HIV-infected people including recipients of bone marrow, cardiac, and renal transplants.(38,39)
| Hairy Leukoplakia and Progression of HIV Disease|
Diagnosis of HL is an indication of both HIV infection and immunodeficiency; it is an indication for a work-up to evaluate and treat HIV disease. HL correlates with a statistical risk for more rapid progression of HIV disease. In an early study, 30% of persons with HL progressed to late-stage HIV disease characterized by CDC-defined AIDS within 36 months.(35) In a later study, 47% of a group developed CDC-defined AIDS within 2 years and 67% within four years.(40) Those persons with HL who progressed to CDC-defined AIDS most rapidly, however, were more often anergic to Candida antigen at diagnosis of HL, indicating significant immunosuppression at that time.(41) Progression to CDC-defined AIDS was more rapid in those HIV-infected persons with HL than in those without HL, even after adjustment for CD4+ T-cell count.(34)
The Epstein-Barr virus (EBV) in HL is both unusual in that deletions in the EBNA 2 gene have been described(42,43) and in that to date no viral DNA is found in the basal layers of HIV.(44,45) Intraepithelial Langerhans' cells (LCs) are reduced or absent in the HL lesion, which correlates with the presence of viral antigens.(46) It is not known whether the lack of LCs is a cause of HL or a consequence of EBV infection.
In electron microscopic specimens, investigators have found structures consistent with a herpes group virus.(42) One structure consisted of 100-nm intranuclear virions and 240-nm encapsulated virus particles. Other structures are 48- to 52-nm particles visible in the suprabasal layer.(47) Closer to specimen surfaces, where the nuclei are more condensed, arrays of these particles and herpes group particles occurred in the same cell.(48) Several studies described the appearance of these particles in HL biopsies.(49,50)
| Clinical Appearance and Manifestations|
HL lesions vary in size and appearance and may be unilateral or bilateral. The surface is irregular and may have prominent folds or projections, sometimes markedly resembling hairs. Occasionally, however, some areas may be smooth and flat. Lesions occur most commonly on the lateral margins of the tongue and may spread to cover the entire dorsal surface (Figure
5). They may also spread downward onto the ventral surface of the tongue, where they usually appear flat. HL lesions can also occur on the buccal mucosa, generally as flat lesions.(48) Rarely, lesions occur on the soft palate.(51) HL usually does not cause symptoms.
| Differential Diagnosis|
Candida albicans may be found in association with many HL lesions, and hyphae can be seen in specimens taken from lesions and examined using potassium hydroxide. Hyphae can be seen in sections stained with periodic acid-Schiff. Administration of antifungal drugs may change the appearance of the lesions but does not cause them to disappear. Clinicians must distinguish them from other white lesions, such as lichen planus, idiopathic leukoplakia, white sponge nevus, dysplasia, and squamous cell carcinoma.
HL should be diagnosed by biopsy for definitive diagnosis. Experienced clinicians can make a presumptive diagnosis of HL in association with HIV disease from the clinical appearance, although HL can be confused with oral candidiasis. The typical microscopic appearance of HL includes acanthosis, marked parakeratosis with the formation of ridges and keratin projections, areas of ballooning cells, and little or no inflammation in the connective tissue. The ballooning changes resemble koilocytosis. Cells are enlarged; some contain enlarged ballooning cells with pyknotic nuclei. Some contain perinuclear haloes.
Definitive diagnosis of HL requires demonstration of EBV.(52) EBV may be readily demonstrated in biopsy specimens by a variety of techniques.(42) Cells taken from the HL lesion by scraping can be used for a noninvasive diagnosis using in situ hybridization.(43)
Hairy leukoplakia usually is asymptomatic and does not require treatment. HL is almost always a manifestation of HIV infection, and clinicians should arrange evaluation of HIV disease and appropriate treatment for patients with HL. HL has disappeared in patients receiving high-dose acyclovir for herpes zoster, presumably because of the anti-EBV activity of acyclovir.(53,54) Doses of acyclovir (2.5 to 3 mg per day for 2 to 3 weeks) usually eliminate HL, but the lesion usually recurs with cessation of treatment.
Elimination or almost complete clinical resolution of the lesion has occurred in patients treated with agents such as desciclovir, an analog of acyclovir,(55) phosphonoformate, Retin A, and podophyllin resin, although lesions tend to recur within a few months. Case reports describe HL disappearing during treatment with ganciclovir, zidovudine, and aerosolized pentamidine.(56) Katz and colleagues have shown that HL both appears and disappears in patients receiving zidovudine,(56) although no case-controlled studies are available.
Occasionally, Candida albicans may be found in HL lesions. Treatment consists of antifungal medications.
| BACTERIAL LESIONS|
| Periodontal Disease|
Periodontal disease is a fairly common problem in both asymptomatic and symptomatic HIV-infected patients.(57,58) It can take two forms: the rapid and severe condition called necrotizing ulcerative periodontitis (NUP)(59) and its associated and possibly precursor condition called linear gingival erythema (LGE).(60) The presenting clinical features of these diseases often differ from those in non-HIV-infected persons.
| Clinical Features|
LGE and NUP often occur in clean mouths where there is very little plaque or calculus to account for the gingivitis. The onset is often sudden, with rapid loss of bone and soft tissue. In LGE, the gingiva may be reddened and edematous (Figure
6). Patients sometimes complain of spontaneous bleeding. In acute-onset ulcerative gingivitis, ulcers occur at the tips of the interdental papilla and along the gingival margins, and often elicit complaints of severe pain. The ulcers heal, leaving the gingival papillae with a characteristic cratered appearance.
NUP may present as rapid loss of supporting bone and soft tissue. Typically, these losses occur simultaneously with no formation of gingival pockets, sometimes involving only isolated areas of the mouth. Teeth may loosen and eventually fall out, but uninvolved sites can appear healthy.(61) Necrotizing stomatitis may develop, and areas of necrotic bone may appear along the gingival margin. The bone may eventually sequestrate. Patients with NUP and necrotizing stomatitis frequently complain of extreme pain and spontaneous bleeding.(62)
| Differential Diagnosis|
The patient's history and clinical appearance make the diagnosis. It is sometimes difficult to distinguish this type of periodontal disease from non-HIV-related periodontal disease. However, the complaints of severe pain, rapid onset, and rapid destruction in an often extremely clean mouth are unusual for non-HIV-related periodontal disease.
Clinicians should refer patients to a periodontist or dentist for management. The following protocol has achieved reasonable success: plaque removal, local debridement, irrigation with povidone-iodine, scaling and root planing, and maintenance with a chlorhexidine mouth rinse (Peridex-R) once or twice daily. Studies show that the addition of chlorhexidine to this regimen produces significant improvement in periodontal condition. In cases of NUP, metronidazole (one 250-mg tablet four times daily), amoxicillin/clavulanate (Augmentin)(one 250-mg tablet three times daily), or clindamycin (one 300-mg tablet three times daily) should be added to the treatment regimen.(63,64)
| Different Course in HIV Infection|
The microbiology(65) of periodontal disease in HIV-infected patients has not been fully described.(63) Oral flora associated with LGE and NUP appear to be similar to those associated with periodontal disease seen in non-HIV-infected persons. Recurrences of acute episodes are common and response to conventional treatment may be poor. However, therapeutic strategies and frequent recall appointments can produce effective local treatment of LGE and NUP.(64) There is as yet no known relationship between these conditions and the progression of HIV disease.
| MYCOBACTERIUM AVIUM-INTRACELLULARE|
One report describes a case of Mycobacterium avium-intracellulare that presented as palatal and gingival granulomatous masses in the oral cavity. A diagnosis of acid-fast bacilli (AFB) was made from a specially stained (acid-fast) biopsy specimen. The AFB cultured from blood and sputum were Mycobacterium avium-intracellulare.(66)
| NEOPLASTIC LESIONS|
| Kaposi's Sarcoma|
Kaposi's sarcoma (KS) may occur intraorally, either alone or in association with skin and disseminated lesions.(67) Intraoral lesions have been reported at other sites and may be the first manifestation of late-stage HIV disease (AIDS). KS occurs most commonly in men but also has been observed in women.(68)
| Clinical Features|
KS can appear as a red, blue, or purplish lesion. It may be flat or raised, solitary or multiple. The most common oral site is the hard palate, but lesions may occur on any part of the oral mucosa, including the gingiva, soft palate, and buccal mucosa (Figure
7), and in the oropharynx. Occasionally, yellowish mucosa surrounds the KS lesion. Oral KS lesions may enlarge, ulcerate, and become infected. Good oral hygiene is essential to minimize these complications.
| Differential Diagnosis|
KS must be distinguished from vascular lesions such as hematomas, hemangiomas, other vascular tumors, pyogenic granulomas, bacillary angiomatosis,(69) and pigmented lesions such as oral melanotic macules. Diagnosis is made from histologic examination.(70,71) There are usually no bleeding problems associated with a biopsy of oral KS. However, aspiration of a lesion prior to biopsy may be useful to rule out a hemangioma. Small, flat lesions are probably in early stages, and the histologic appearance is different from the larger, nodular lesions that are probably more advanced. Early lesions may be difficult to diagnose histologically because they resemble endothelial proliferation. KS may appear suddenly, within days of a normal oral examination, in previously uninvolved areas of the mouth.
Providers should ensure that a patient with KS receives evaluation and follow-up care for the underlying HIV disease.(68)
Treatment is determined on the basis of the number, size, and location of the oral KS lesions. The choice of therapy depends on the effect of treatment on the adjacent mucosa, pain associated with treatment, interference with eating and speaking, and the patient's preference. It is important to perform thorough dental prophylaxis before initiating therapy for KS lesions involving the gingiva. Response to therapy is improved if all local plaque and calculus are removed. Local application of sclerosing agents may reduce the size of oral lesions.(72)
Local treatment is appropriate for large oral KS lesions that interfere with eating and talking.(72,73) Oral KS can be treated surgically or with localized intralesional chemotherapy. Surgical removal is suitable for small, well-circumscribed lesions such as gingival or tongue lesions. Surgical removal can be performed under local anesthesia with a blade or with the carbon dioxide laser. Intralesional vinblastine is useful for treating small lesions, particularly on the palate or gingiva. Several studies have documented the effectiveness of one or two injections of 0.1 to 0.2 mg per ml solution of vinblastine. Posttreatment pain is fairly common, but systemic effects are rare.(73) The pain usually disappears several days after therapy.
Radiation therapy may be indicated for large, multiple lesions.(70) A single dose of 800 cGy or an equivalent fractionated dose is frequently used and produces a good response. Side effects include xerostomia and mucositis,(74) although both conditions usually improve with cessation of radiation therapy.
| Clinical Features|
Diffuse, undifferentiated non-Hodgkin's lymphoma (NHL) is a frequent HIV-associated malignancy.(75,76) Most are of B cell origin, and Epstein-Barr virus occurs in cells from several cases. Lymphoma can occur anywhere in the oral cavity,(77) and there may be soft tissue involvement with or without involvement of underlying bone. The lesion may present as firm, painless swelling that may be ulcerated. Some oral lesions may appear as shallow ulcerations.(78) Oral NHL may appear as solitary lesions with no evidence of disseminated disease.
| Differential Diagnosis|
Oral NHL may be confused with major aphthous ulcers and rarely as a pericoronitis associated with an erupting third molar. Diagnosis of NHL must be made by histologic examination of biopsy specimens.
After diagnosis of the oral lesions, the patient must be referred for further evaluation for disseminated disease and its subsequent treatment.
| OTHER ORAL LESIONS ASSOCIATED WITH HIV DISEASE|
| Salivary Gland Disease and Xerostomia|
Salivary gland disease associated with HIV infection (HIV-SGD) can present as xerostomia with or without salivary gland enlargement.(84) Reports describe salivary gland enlargement in children and adults with HIV infection usually involving the parotid gland. The enlarged salivary glands are soft but not fluctuant. In some cases, enlarged salivary glands may be due to lymphoepithelial cysts.(85) Schiodt et al. found that 9 of 12 patients (11 adults and 1 child) with HIV-SGD had salivary gland enlargement. Three had xerostomia. Labial salivary gland biopsy revealed histologic features similar to those in Sjogren's syndrome.(84) In HIV-SGD, however, the lymphocytic infiltrate is predominantly CD8 cells, unlike that in Sjogren's syndrome, which is predominantly CD4 cells.(76)
No evidence of Epstein-Barr virus or cytomegalovirus has been found in biopsies of salivary glands.(86) One report describes an association between HIV-SGD and HLA-DR5 and HLA-B35 cell-surface antigen.(87)
The etiology of HIV-SGD is as yet unknown but the enlarged parotid glands can be a source of annoyance and discomfort.
Xerostomia is sometimes seen in individuals with HIV-SGD. HIV-infected patients may also experience dry mouth in association with taking certain medications that can hinder salivary secretion, such as ddI, antidepressants, antihistamines, and antianxiety drugs.
Removal of the enlarged parotid glands is rarely recommended. For individuals with xerostomia, the use of salivary stimulants such as sugarless gum or sugarless candies may provide relief. Candies that are acidic should be avoided as frequent use may lead to loss of tooth enamel. The use of salivary substitutes may also be helpful. An increase in caries can occur, so fluoride rinses (that can be bought over the counter) should be used daily, and visits to the dentist should occur two to three times per year.
|| ||Greenspan D, Greenspan JS, Schiodt M, et al. AIDS and the mouth. Copenhagen: Munksgaard, 1990.|
|| ||Akova M, Akalin HE, Uzun O, et al. Emergence of Candida krusei infections after therapy of oropharyngeal candidiasis with fluconazole. Eur J Clin Microbiol Infect Dis 1991;10:598-9.|
|| ||Murray PA, Holt S. Microbiology of HIV-associated gingivitis and periodontitis. In: Robertson PB, Greenspan JS, eds. Oral manifestations of AIDS. Littleton, Mass.: PSG Publishing, 1988.|
|| ||Grassi M, Williams CA, Winkler JR, et al. Management of HIV-associated periodontal diseases. In: Robertson PB, Greenspan JS, eds. Oral manifestations of AIDS. Littleton, Mass.: PSG Publishing, 1988.|
|| ||Greenspan JS, Silverman S Jr, Greenspan D. HIV infection and oral cancer. IV International Conference on AIDS. Stockholm, 1988;2:2663.|